← Back to catalogue

Fentex

FDA UDI

Class I (US FDA UDI)

by FENTEX medical GmbH

Identity

Trade Name
FENTEX FDA UDI
Generic Name
Rhinoscopic mirror FDA UDI
Device Name
Rhinoscopic Mirror by Michel 27 cm, size 1 FDA UDI
Model / Reference
054212FX FDA UDI
Description
Rhinoscopic Mirror by Michel 27 cm, size 1 FDA UDI

Identifiers

Catalog Number
054212FX FDA UDI
Primary DI / UDI-DI
04250407706456 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Rhinoscopic mirror FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rhinoscopic mirror

Fentex by FENTEX medical GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rhinoscopic mirror.

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
FENTEX medical GmbH

Sources (1)

  • FDA UDI 63197342-5f62-4010-9590-ce7df8f6afb1 35 fields · synced May 30, 2026