Fentex

FDA UDI

Class I (US FDA UDI)

by FENTEX medical GmbH

Identity

Trade Name: FENTEX FDA UDI
Generic Name: Surgical cutting/shaping board, reusable FDA UDI
Device Name: Cutting Block made of Glas, one side silk finish 80 x 100 x 6 mm FDA UDI
Model / Reference: 169730FX FDA UDI
Description: Cutting Block made of Glas, one side silk finish 80 x 100 x 6 mm FDA UDI

Identifiers

Catalog Number: 169730FX FDA UDI
Primary DI / UDI-DI: 04250407772604 FDA UDI
FDA Product Code: LRC FDA UDI
GMDN Term: Surgical cutting/shaping board, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical cutting/shaping board, reusable

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

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Also classified as Surgical cutting/shaping board, reusable.

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MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
Preparation tray, stainless steel — Spiggle & Theis Medizintechnik GmbH · Class I
Gyrus ACMI — Gyrus Acmi, Inc. · Class I
V. Mueller — STERIS CORPORATION · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: FENTEX medical GmbH

Sources (1)

FDA UDI cb380436-8a37-4ee1-90d8-7fde080d0341 35 fields · synced May 30, 2026