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Fentex

FDA UDI

Class I (US FDA UDI)

by FENTEX medical GmbH

Identity

Trade Name
FENTEX FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
Operating Laryngoscope by Jackson for children, with light carrier 17 cm FDA UDI
Model / Reference
530302FX FDA UDI
Description
Operating Laryngoscope by Jackson for children, with light carrier 17 cm FDA UDI

Identifiers

Catalog Number
530302FX FDA UDI
Primary DI / UDI-DI
04250407741198 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Rigid optical laryngopharyngoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 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: Rigid optical laryngopharyngoscope

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

Similar devices

Also classified as Rigid optical laryngopharyngoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
FENTEX medical GmbH

Sources (1)

  • FDA UDI 3cb7f75b-d80f-4483-ae09-ba429286ebcb 35 fields · synced Jun 1, 2026