Widely Compatible to Third Party Resin

Quickly access to various new materials on the market!

 

 

 

 

MiiCraft BV Resins For Different Applications

 

Model NumberModel NamePrint-out featuresPrint-out examplesApplication
BV002AModel Black



Fine and precise printing parts. Materials for high resolution rapid prototyping.Rapid prototyping
BV007AMicro-structure TransparentSuitable for printing microchannel and any parts requiring translucency.Micro smallMicrofluidics, Transparent parts
BV005ADental Model CaramelPrecise and matte surface printing parts, suitable for surface detail checking. Economical choice.Dental model,Rapid prototyping
BV006ADental Model WhitePrecise and smooth surface printing parts. Economical choice.Dental model,Rapid prototyping
BV013AJewelry Cast HDCastable and high resolution printing parts, also excellent in its casting results.bv013Jewelry(Castable)
BV022IP High-ResistantToughness and maintain flexibility. Impact resistant.Functional Parts & Rapid Prototyping
BV023IP Durable BlackStrong and durable printing parts, able to undergo periods of stress or strain.Engineering, Functional Parts & Rapid Prototyping

Click here to download suggested curing time for above resins or check printing parameters here

Third Party resins

BASF X004M, Transparent. Fulfill the requirements of functional applications regarding high accuracy and mechanical strength.

 

 

 

 

Biocompatible resins

We offer a wide variety of biocompatible resins compatible with MiiCraft printers.

KeyPrint, a leading developer and manufacturer of biocompatible materials for dentistry

Check KeyPrint materials here

 

NextDent B.V., a leading developer and manufacturer of biocompatible materials for dentistry

Check NextDent materials here

 

 

 

 

*Materials with Class I and Class IIa certification according to the Medical Device Directive 93/42/EC

DETAX GmbH, a leading developer and manufacturer of biocompatible materials for dentistry
Check DETAX materials here

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*Materials with Class I and Class IIa certification according to the Medical Device Directive 93/42/EC

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