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Gingivamoll pink 5g

FDA UDI

Class I (US FDA UDI)

by DETAX GmbH

Identity

Trade Name
Gingivamoll pink 5g FDA UDI
Generic Name
Cosmetic silicone-liquid tissue reconstructive material FDA UDI
Model / Reference
03023 FDA UDI

Identifiers

Primary DI / UDI-DI
EDET030231 FDA UDI
FDA Product Code
NOK FDA UDI
GMDN Term
Cosmetic silicone-liquid tissue reconstructive material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3800 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

No

FDA UDI

Gingivamoll pink 5g by DETAX GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DETAX GmbH

Sources (1)

  • FDA UDI e842e8e1-e3e6-43f2-876c-c73c4836304f 33 fields · synced May 31, 2026