| HS Code | 367897 |
| Product Name | 3D Systems VisiJet RCL-ENT-A40 Multi-Material Composites (VisiJet CR-CL 200 + VisiJet CE-NT) |
| Material Type | Multi-Material Composite |
| Composition | VisiJet CR-CL 200 + VisiJet CE-NT |
| Tensile Strength | 8.5 MPa |
| Tensile Modulus | 10 MPa |
| Elongation At Break | 150% |
| Flexural Strength | 2 MPa |
| Flexural Modulus | 10 MPa |
| Hardness | 40 Shore A |
| Izod Impact Strength | 200 J/m |
| Heat Deflection Temperature | 35 °C |
| Density | 1.11 g/cm³ |
| Tear Strength | 10 kN/m |
| Water Absorption | 0.3% |
| Color | Translucent |
As an accredited 3D Systems VisiJet RCL-ENT-A40 Multi-Material Composites (VisiJet CR-CL 200** + VisiJet CE-NT) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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In the fabrication of craniomaxillofacial surgical planning models, VisiJet RCL-ENT-A40 is deployed as a two-phase construct in which VisiJet CR-CL 200** forms the rigid cortical bone analogue and the CE-NT-dominant A40 digital material forms the compliant soft-tissue analogue. The design file is not a homogeneous blend but a voxel-level material assignment; the production process relies on the MJP printhead delivering separate melt streams of CR-CL 200** and CE-NT, with the A40 profile generated by a fixed droplet ratio established in the build preparation software. For the rigid phase, the assignment is 100% CR-CL 200**; for soft-tissue structures, the assignment is the A40 profile with nominal Shore A 40 hardness measured according to ASTM D2240-15e1. If a transitional fibrocartilage-like region is required, the software can generate an intermediate digital material by altering the CE-NT/CR-CL 200** droplet fraction, but the exact addition ratio for the A40 designation is not published as an offline compounding formula. Compliance documentation for non-sterile pre-production surgical simulators is maintained under ISO 13485:2016, while biological evaluation is referenced to ISO 10993-1:2018 with testing per ISO 10993-5:2009 and ISO 10993-10:2010 only when the printed model is intended for tissue-contact simulation; because the unpainted composite is not sterilized and is not cleared for permanent patient contact, the technical file must record this boundary. Downstream production begins with DICOM segmentation from CT or MR data, followed by surface reconstruction, digital material assignment, and printing in an MJP system with a sacrificial wax support phase. Supports are removed with a heated bath, and the model is then subjected to dimensional inspection using a structured-light scanner or CMM; tensile verification of the rigid phase follows ASTM D638-14, while the elastomer phase is characterized under ASTM D412-16. Terminal finished parts in this application include patient-specific anatomical simulators, surgical navigation reference models, and pre-contoured plate positioning mockups used by craniomaxillofacial teams.
Automotive electrical connector development requires a seal geometry that remains attached to a rigid connector housing during repeated mating and unmating, and VisiJet RCL-ENT-A40 addresses this by printing the housing and seal in a single build rather than overmolding the elastomer onto a moulded thermoplastic body. The housing is assigned 100% VisiJet CR-CL 200**; the seal bead is assigned the A40 digital material profile, which deposits the CE-NT-dominant blend at nominal Shore A 40 per ASTM D2240-15e1. The formulation addition ratio is therefore not a batch weight percentage but a printer-defined jetting ratio between CE-NT and CR-CL 200** across the seal voxels; where a firmer retention collar is required, the build software can select a lower CE-NT fraction from the digital material set. Compliance verification for automotive interior and engine-compartment-adjacent prototypes should reference ISO 3795 for burning rate, DIN 75201 for fogging behaviour, and SAE/USCAR-2 for connector system performance. Published data for the A40 blend specifically under full USCAR-2 thermal cycling and vibration exposure are limited, so pre-production validation must run connector-specific pressure-decay leak tests and thermal ageing rather than relying on generic supplier datasheets. The downstream process begins with connector CAD geometry separating housing and seal bodies, followed by MJP digital material assignment and simultaneous printing of the rigid and elastomer phases. Wax support removal is performed in a heated bath, after which the connector is dried and subjected to insertion-force measurement and environmental cycling. Terminal finished outputs include sealed electrical connector prototypes, HVAC actuator soft-touch seals, and grommet assemblies for body-panel pass-throughs.
Overmolded consumer electronics prototypes—wearable bands, hearing aid housing cushions, and augmented-reality facial interfaces—require a rigid chassis segment and a soft elastomer segment without secondary adhesive operations. In this build strategy, the rigid frame is produced from 100% VisiJet CR-CL 200**, and the skin-contact band is produced from the A40 profile, which is a CE-NT-dominant digital material with a nominal Shore A 40 hardness measured per ASTM D2240-15e1. The addition ratio for the A40 region is managed as a voxel-level droplet fraction of CE-NT to CR-CL 200** delivered through separate MJP printhead channels; no offline mixing, no precision weighing, and no twin-screw compounding is performed at the fabricator level. Compliance testing for the completed prototype is typically evaluated against IEC 62368-1:2018 for information technology and communication equipment, with flammability classification referenced to UL 94 HB or UL 94 V-2 as applicable; mechanical verification of the rigid phase follows ASTM D638-14, and the elastomer segment follows ASTM D412-16. Downstream production includes CAD assignment of rigid and A40 material regions, MJP printing with a wax support phase, support removal by melting, and an isopropanol rinse to remove residual support film. Because the elastomer segment is printed directly onto the rigid frame, the failure mode of adhesive delamination at the band-to-chassis interface is eliminated, but the process boundary is that the as-printed surface can retain trace wax in deep undercuts if support removal time is shortened. Terminal finished parts include functional wearable product prototypes, watch strap and housing mockups, and facial interface assemblies for ergonomic assessment.
| Application scenario | Reference standard / test method | Measured attribute | Specimen configuration |
|---|---|---|---|
| Medical model rigid phase | ASTM D638-14 | Tensile strength, modulus | Type IV specimen, thickness 3.2 mm |
| Elastomer phase / A40 | ASTM D412-16 | Tensile strength, elongation at break | Die C, thickness 2.0 mm ± 0.1 mm |
| Hardness verification | ASTM D2240-15e1 | Shore A | Plaque thickness 6.0 mm, reading at 15 s |
| Automotive interior flammability | ISO 3795 | Burning rate | Flat specimen, edge ignition |
| Elastomer fluid resistance | ISO 1817:2015 | Volume change after immersion | Reference fluid, time/temperature per fluid class |
| Footwear compression set | ISO 815-1:2014 | Compression set | Type B moulded test piece, 25% compression |
For industrial fluid handling component validation, short-run functional assemblies require a rigid valve body and a deformable diaphragm that can withstand cyclic air or water pressure without adhesive-bonded interfaces. The diaphragm is assigned the A40 profile, a CE-NT-dominant digital material with nominal Shore A 40 hardness per ASTM D2240-15e1; the valve body and threaded coupling ring are assigned 100% VisiJet CR-CL 200**. The addition ratio for the A40 diaphragm is a printer-defined volumetric droplet ratio between CE-NT and CR-CL 200**, not a conventional phr addition level, and the exact ratio is not published for stand-alone compounding. Compliance testing for rigid tensile properties follows ISO 527-2:2012, elastomer tensile and elongation follow ASTM D412-16, fluid resistance follows ASTM D471-16a and ISO 1817:2015, and potable-water contact requires extractables evaluation under FDA 21 CFR 177.2600 or equivalent regional regulation; the as-printed MJP polymer is not presumed food-contact compliant without application-specific extraction testing. The downstream process involves printing the valve body and diaphragm in a single build, removing the wax support phase by heating, drying to constant mass, and then conducting a low-pressure pneumatic cycling test at pressures defined by the valve seat area and diaphragm thickness. A recognized process bottleneck occurs when the diaphragm thickness is below the minimum feature size recommended by the printer manufacturer for support removal, because residual wax in the convolute can alter effective stiffness and produce false leak rates; published data for this specific configuration are limited, so fabricators should characterise first-article parts with opening-pressure and hysteresis measurements. Terminal finished parts include diaphragm valve prototypes, metering pump chamber assemblies, and gasket-sealed filter housing test units.
Because footwear and orthotic compression zones are subject to cyclic compressive loading, the rigid anti-torsion plate and the compression zones can be produced as one multi-material print, eliminating direct injection moulding tooling for each iteration of heel and metatarsal padding. The anti-torsion region is assigned 100% VisiJet CR-CL 200**; the compression cells are assigned the A40 digital material profile with nominal Shore A 40 hardness per ASTM D2240-15e1. Addition ratio in this application is not a post-hoc blending operation; the MJP software sets the CE-NT/CR-CL 200** droplet ratio for the A40 compression phase, and the fabricator selects the profile rather than weighing out resin components. Rebound and compression behaviour are evaluated under ISO 815-1:2014 for compression set, ASTM D575-91 for compression-deflection, ASTM D412-16 for elastomer tensile properties, and ISO 868:2003 for Shore hardness verification. Downstream production uses a digital last or 3D scanned foot form, a lattice or solid-modelled orthotic body, and MJP printing of the rigid plate and A40 compression cells with wax support removal. Because the build envelope of the MJP system can limit full-sole prototypes to smaller sizes, the part may be segmented along the arch line and bonded after printing; this segmentation introduces an adhesive layer that is not part of the original material system and must be validated separately. Terminal finished products include multi-density orthotic insoles, heel-pad prototypes for footwear brands, and load-distribution wedges used in sports shoe development.
When orthodontic appliance verification and dental teaching models require a clear rigid tooth analogue with a resilient gingival mask, the transparent rigid phase represents enamel and the A40 elastomer phase represents gingival tissue, permitting aligner thermoforming workflows that must distinguish between hard and soft structures in the same model. The dentition is assigned 100% VisiJet CR-CL 200**; the gingival mask is assigned the A40 profile, a CE-NT-dominant digital material with nominal Shore A 40 hardness per ASTM D2240-15e1. The formulation addition ratio is configured in the MJP build software as a voxel-level CE-NT/CR-CL 200** droplet fraction, not as a laboratory compounding step. Non-patient-contact dental models are not classified as medical devices in most jurisdictions, but laboratories operating under ISO 13485:2016 use ISO 10993-1:2018 as a risk-assessment reference and document that the printed part does not enter the mouth. The downstream process includes intraoral scan or stone model digitisation, segmentation of tooth crowns from gingiva, assignment of build materials, direct printing of the multi-material model, wax support removal, and final articulation. The elastomeric gingiva permits repeated seating and removal of aligner staging sheets without fracture of the rigid tooth analogue; however, the as-printed elastomer phase is not intended for prolonged intraoral contact, and the technical record must specify that the model is for laboratory use only. Terminal finished outputs include diagnostic setup models, clear aligner staging models, and dental laboratory training replicas.
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3D Systems VisiJet RCL-ENT-A40 Multi-Material Composites is a two-phase photopolymer set identified by the combination of VisiJet CR-CL 200** and VisiJet CE-NT. Unlike single-cartridge photopolymer resins that produce monolithic parts, the RCL-ENT-A40 set is configured for material jetting platforms capable of dispensing two distinct photopolymers into one build sequence. The A40 designation in the manufacturer nomenclature indicates a nominal durometer target of 40 Shore A for the CE-NT phase when evaluated according to ASTM D2240-15e1. The CR-CL 200** phase is specified as a clear rigid photopolymer, while the CE-NT phase provides elastomeric behavior for sealing, gripping, and strain-absorbing features. Published data for this specific configuration is limited; mechanical property statements should therefore be obtained from lot-specific certificates of analysis and not from generic acrylate photopolymer documents. The primary usage is in multi-material prototypes and short-run production parts where a rigid clear region must be integrated with a flexible region without adhesive bonding or mechanical assembly. Representative application areas include fluidic devices with transparent inspection windows, medical device housings with soft-touch overmolds, and consumer electronics enclosures that require localized elastomer seals. Each application requires validation of the finished part under the relevant end-use standards, because the phase boundary rather than either bulk material may dominate long-term performance.
The set contains two distinct jettable photopolymer phases. VisiJet CR-CL 200** functions as the rigid structural phase. Its clarity supports optical path requirements, and its higher crosslink density contributes to dimensional stability in load-bearing features. VisiJet CE-NT functions as the elastomeric phase. The A40 suffix is associated with a nominal hardness of 40 Shore A, placing it in the soft-flexible range rather than the semi-rigid range. Compared with VisiJet M2R-CL, a single clear rigid material, the RCL-ENT-A40 set introduces a controlled material discontinuity that can reduce assembly part count but requires explicit interfacial qualification. Compared with VisiJet M2G-DUR, which is a single durable rigid material, the two-phase set offers spatial modulation of stiffness rather than a homogeneous toughness improvement. When the two phases are jetted in alternating or graded patterns, the mechanical response depends on the printed phase volume fraction, feature size, and transition topology. The material set does not behave as a miscible blend; it forms a bonded composite with a finite interphase zone. The thickness of that interphase zone is influenced by jetted layer thickness, UV dose, and the surface conversion state of the previously jetted layer. Because the exact interphase thickness is not published for all build modes, it should be measured on cross-sectioned coupons using optical or scanning electron microscopy.
| Characterization requirement | Applicable phase | Standard designation | Notes |
|---|---|---|---|
| Durometer hardness | CE-NT phase | ASTM D2240-15e1, Type A | Lot-specific certificate required |
| Tensile properties | CR-CL 200** phase | ASTM D638-14 / ISO 527-2:2012 | Dried specimens |
| Tear resistance | CE-NT phase | ASTM D624-00(2020) Type C | Nicked specimen configuration |
| Heat deflection | CR-CL 200** phase | ASTM D648-18 Method B at 0.455 MPa | Condition per standard |
| Water absorption | Both phases | ISO 62:2008 | Compare at saturation |
| Cytotoxicity | Finished device use | ISO 10993-5:2009 | Required for medical or skin-contact use |
In production-scale material jetting equipment, the RCL-ENT-A40 cartridges are maintained in temperature-controlled bays with recirculation loops. Piezoelectric printheads jet the two phases according to layer-wise bitmaps generated from the CAD model. Build layer thickness is equipment-specific and must be selected from the validated process set; published data for this specific configuration is limited for unsupported layer heights. The rigid phase and elastomeric phase must be matched for jetted drop volume, UV penetration, and substrate wetting. If the CE-NT phase is jetted onto a partially cured CR-CL 200** surface, residual reactive species at the interface can promote covalent bonding. Conversely, overexposure of the clear rigid phase can reduce residual acrylate groups and shift failure toward adhesive delamination. Batch-to-batch viscosity drift in the CE-NT phase alters drop velocity and may create interface misregistration. Inline filtration at 1–5 µm is commonly used to prevent nozzle clogging, but the filtration efficiency must be confirmed for the elastomeric phase because high-viscosity materials can exhibit shear-induced filtration effects. Jetting instability in production lines is most often observed as missing jets, satellite droplets, or periodic interface voids. These defects are not reliably detected by visual inspection alone; automated vision systems or mass-based density checks are required for critical parts.
The mechanical continuity of RCL-ENT-A40 parts depends on the cure gradient across the transition zone. UV irradiance attenuates through the transparent rigid phase and is scattered by the elastomeric phase; the result is a non-uniform conversion of acrylate double bonds. Interface strength is evaluated by destructive testing on representative coupons. Peel resistance may be measured according to ASTM D6862-11, while lap shear specimens can follow ASTM D3163-01(2023). These standards provide comparative data when specimen geometry and conditioning are kept constant; they do not remove the need for lot-specific validation. The difference between the rigid phase’s high crosslink density and the elastomeric phase’s lower crosslink density creates a modulus divergence that concentrates stress near the jetted interface. Parts with abrupt transitions are therefore more likely to delaminate under flexural fatigue than parts with graded transition regions. Production-scale lines have exhibited edge delamination when the elastomeric phase is jetted at lower temperatures, because viscosity increases reduce wetting and diffusion into the rigid phase surface. Use of heated build chambers can reduce this risk, but the chamber temperature must remain below the CE-NT phase thermal deflection limit. For fluid-exposed parts, the elastomeric phase may swell more than the rigid clear phase. Swelling mismatch creates shear stress along the interface and can reduce tensile strength. Qualification for fluid handling applications should include immersion testing per ISO 62:2008 followed by tensile testing to ASTM D638-14, with mass change and dimensional change recorded at 24 h and 168 h. Without this data, the assumption that the rigid phase dominates solvent resistance is not supported. The interface should also be inspected after thermal cycling because differential expansion between the phases can generate microcracks. A thermal cycle from −20 °C to 60 °C is a useful screening profile for general-purpose prototypes, but the final profile must match the intended use environment.
Cartridge temperature stability defines the lower and upper processing boundaries for the CE-NT phase. If the resin temperature falls below the manufacturer-specified jetting window, dynamic viscosity rises and the piezoelectric printhead may produce satellite droplets or missing nozzles. On a production line, this condition appears as periodic interface voids and a loss of Shore A repeatability within a batch. If the temperature exceeds the upper boundary, the CE-NT phase may begin thermal-oxidative degradation, shifting its durometer upward and reducing elongation at break. Operators should monitor the recirculation system’s temperature sensors and heater output against the material-specific setpoint. Thermal deviation alarms should trigger a jetting pause and a test coupon print. The coupon set is typically evaluated by ASTM D2240-15e1 for hardness, ASTM D638-14 for tensile properties, and cross-sectional microscopy for void density. If the void count exceeds the internal acceptance limit, the batch should be purged and the printhead cleaned. Because published data for this specific configuration is limited, the acceptable temperature range must be taken from the current VisiJet RCL-ENT-A40 handling documentation and not from generic UV resin guidance. In addition, the temperature of the build platform should be controlled independently, because thermal gradients across thick multi-material sections can produce warpage at the phase boundary. When thick rigid sections are adjacent to elastomeric regions, a slower cool-down after build completion reduces residual stress. The cool-down protocol should be documented as part of the process recipe. Any change in cartridge lot should be accompanied by a small batch build that includes a standardized interface test coupon and a Shore A hardness coupon. The acceptance limits for these coupons should be derived from baseline data collected on the same machine, not from values transferred from a different material jetting system.
After the build cycle, support removal for VisiJet RCL-ENT-A40 parts typically requires controlled heating of the wax support phase. The upper temperature of the support removal oven must remain below the CE-NT phase thermal oxidative threshold. If the temperature is set too high, the elastomeric phase can show a permanent hardness increase that is detectable by ASTM D2240-15e1 and a corresponding loss in elongation at break. The rigid CR-CL 200** phase is less sensitive to short thermal excursions, but long exposure can accelerate yellowing and reduce transmission clarity. For clear regions that require optical performance, transmission haze should be checked according to ISO 13468-1:2019 or an equivalent spectrophotometric method. Residual wax left in internal channels is a common failure source in fluidic prototypes; automated melting with controlled airflow reduces this risk, but blind channels require validated drainage. After support removal, the parts may require a UV post-cure. The post-cure dose should be delivered uniformly to all surfaces; shadowed regions near the interface may cure to a lower conversion and exhibit lower mechanical strength. Parts with large flat rigid sections and thin elastomer features should be supported to prevent distortion during the thermal steps. Dimensional tolerance should be verified by structured-light scanning or CMM, with particular attention to step height at the material boundary. A practical tolerance band for the interface location should be determined on a per-machine basis. Published data for this specific configuration is limited; therefore, generic post-cure recipes from single-phase materials should not be transferred without validation.
Compared with single-material photopolymers and thermoplastic elastomer molding, the RCL-ENT-A40 set differs in that both phases are jetted in the same build and are cured as a thermoset network. The cured composite cannot be remelted or mechanically recycled in the same manner as injection molding regrind. This thermoset nature limits repair by solvent welding, although localized surface bonding may be possible with compatible adhesives after abrasion and cleaning. The material set may be subject to REACH registration and RoHS 2011/65/EU obligations; finished-device manufacturers should verify the latest SDS and compliance statement. For medical or skin-contact applications, cytotoxicity testing per ISO 10993-5:2009 is not automatically satisfied by the resin classification and must be performed on the finished part after support removal and any post-cure. The use of ISO 527-2:2012 tensile testing for the rigid phase and ASTM D2240-15e1 durometer testing for the elastomeric phase provides a minimum comparative framework, but it does not replace application-specific durability testing under load, temperature, and chemical exposure. Because the phase interface is the least predictable element, inspection plans should include cross-sectional microscopy at a defined magnification and frequency. Lot acceptance should be based on the complete process chain from cartridge conditioning through post-cure, not on a single material property.