← Back to catalogue

addition yellow 2 x 660g

FDA UDI

Class I (US FDA UDI)

by DETAX GmbH

Identity

Trade Name
addition yellow 2 x 660g FDA UDI
Generic Name
Earmould impression material FDA UDI
Model / Reference
02399 FDA UDI

Identifiers

Primary DI / UDI-DI
EDET023991 FDA UDI
FDA Product Code
ESD FDA UDI
GMDN Term
Earmould impression material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.3300 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

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

Category: Earmould impression material

addition yellow 2 x 660g by DETAX GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Earmould impression material.

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
DETAX GmbH

Sources (1)

  • FDA UDI b3ff3e35-81f0-4726-9c50-31c5c2485edf 32 fields · synced Jun 1, 2026