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PRO3DURE GR-21 Try-In

FDA UDI

Class I (US FDA UDI)

by Pro3Dure Medical

Identity

Trade Name
PRO3DURE GR-21 Try-In FDA UDI
Generic Name
Dental base plate FDA UDI
Device Name
printodent GR-21 Try-In 1kg ; color:A2 FDA UDI
Model / Reference
1kg FDA UDI
Description
printodent GR-21 Try-In 1kg ; color:A2 FDA UDI

Identifiers

Primary DI / UDI-DI
EPRCD1001601 FDA UDI
FDA Product Code
EEA FDA UDI
GMDN Term
Dental base plate FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

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 base plate

PRO3DURE GR-21 Try-In by Pro3Dure Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental base plate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pro3Dure Medical

Sources (1)

  • FDA UDI 1abe3c0d-570a-443d-99c2-17880de876fc 35 fields · synced May 30, 2026