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printodent GR-10 guide I MSI

FDA UDI

Class U (US FDA UDI)

by Pro3Dure Medical

Identity

Trade Name
printodent GR-10 guide I MSI FDA UDI
Generic Name
Dental appliance fabrication material, resin FDA UDI
Device Name
printodent GR-10 guide I MSI 1000g ; ocean-blue FDA UDI
Model / Reference
1000g ; ocean-blue FDA UDI
Description
printodent GR-10 guide I MSI 1000g ; ocean-blue FDA UDI

Identifiers

Catalog Number
D1000808 FDA UDI
Primary DI / UDI-DI
EPRCD1000808 FDA UDI
510(k) Number
K231775 FDA UDI
FDA Product Code
MQC FDA UDI
GMDN Term
Dental appliance fabrication material, resin FDA UDI

Classification

Device Class
U 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

printodent GR-10 guide I MSI by Pro3Dure Medical — Class U — 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

K231775 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Pro3Dure Medical

Sources (1)

  • FDA UDI bcad6192-f281-4e9d-b5c6-cd6b0896939b 35 fields · synced May 30, 2026