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3Delta Denture Teeth

FDA UDI

Class II (US FDA UDI)

by DeltaMed GmbH

Identity

Trade Name
3Delta Denture Teeth FDA UDI
Generic Name
Resin artificial teeth FDA UDI
Device Name
3Delta Denture Teeth A1 1000g FDA UDI
Model / Reference
1612010 FDA UDI
Description
3Delta Denture Teeth A1 1000g FDA UDI

Identifiers

Catalog Number
1612010 FDA UDI
Primary DI / UDI-DI
EDEL16120100 FDA UDI
FDA Product Code
PZY FDA UDI
GMDN Term
Resin artificial teeth FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Resin artificial teeth

3Delta Denture Teeth by DeltaMed GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resin artificial teeth.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DeltaMed GmbH

Sources (1)

  • FDA UDI 3ed62a0e-b4c3-4a2c-8ccb-adf26d105be6 35 fields · synced Jun 8, 2026