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UCAN Print Base

FDA UDI

Class II (US FDA UDI)

by Pro3Dure Medical

Identity

Trade Name
UCAN Print Base FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
UCAN Print Base 1000g color 33 FDA UDI
Model / Reference
1000g ; color 33 FDA UDI
Description
UCAN Print Base 1000g color 33 FDA UDI

Identifiers

Catalog Number
768345 FDA UDI
Primary DI / UDI-DI
EPRC768345 FDA UDI
510(k) Number
K210298 FDA UDI
FDA Product Code
EBI FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3760 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental appliance fabrication material, resin

UCAN Print Base by Pro3Dure Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pro3Dure Medical

Sources (1)

  • FDA UDI 8af04ebf-531f-4e8d-be18-5ef256dc2a47 35 fields · synced May 30, 2026