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impression plugs, conical

FDA UDI

Class I (US FDA UDI)

by DETAX GmbH

Identity

Trade Name
impression plugs, conical FDA UDI
Generic Name
Earmould impression kit FDA UDI
Model / Reference
03321 FDA UDI

Identifiers

Primary DI / UDI-DI
EDET033211 FDA UDI
FDA Product Code
ESD FDA UDI
GMDN Term
Earmould impression kit 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 kit

impression plugs, conical by DETAX GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Earmould impression kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DETAX GmbH

Sources (1)

  • FDA UDI b8593508-8dc3-47f6-bbbe-f17df4c22c4d 32 fields · synced May 30, 2026