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Fentex

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 535912FXModel Instrument zum Halten, Fassen oder Schneiden.

by FENTEX medical GmbH

Identity

Trade Name
FENTEX FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI
Device Name
Laryngoscopy- and Bronchoscopy Forceps for children, straight, oval cupped WL 35 cm, sheath Ø 1.5 mm FDA UDI
Model / Reference
535912FX EUDAMEDFDA UDI
Instrument zum Halten, Fassen oder Schneiden. EUDAMED
Description
Laryngoscopy- and Bronchoscopy Forceps for children, straight, oval cupped WL 35 cm, sheath Ø 1.5 mm FDA UDI

Identifiers

Catalog Number
535912FX FDA UDI
Primary DI / UDI-DI
04250407743543 EUDAMEDFDA UDI
Basic UDI-DI
B-04250407743543 EUDAMED
FDA Product Code
LRC FDA UDI
EMDN Code
L140399 LARYNX SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical soft-tissue manipulation forceps, alligator, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
874.4420 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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: Surgical soft-tissue manipulation forceps, alligator, reusable

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, alligator, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FENTEX medical GmbH

Sources (2)

  • FDA UDI e76686aa-f472-47c4-99ea-89a6bde2a2d6 35 fields · synced Oct 8, 2026
  • EUDAMED c4617146-2116-489a-b7ea-b2c4e19da512 61 fields · synced Oct 8, 2026