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Fentex

FDA UDI

Class II (US FDA UDI)

by FENTEX medical GmbH

Identity

Trade Name
FENTEX FDA UDI
Generic Name
Rigid endoscope telescope FDA UDI
Device Name
Hi-View Telescope autoclavable 70°, WL 110 mm, Ø 2.7 mm FDA UDI
Model / Reference
728570FX FDA UDI
Description
Hi-View Telescope autoclavable 70°, WL 110 mm, Ø 2.7 mm FDA UDI

Identifiers

Catalog Number
728570FX FDA UDI
Primary DI / UDI-DI
04250407750657 FDA UDI
FDA Product Code
EOB FDA UDI
GMDN Term
Rigid endoscope telescope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4760 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscope telescope

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

Similar devices

Also classified as Rigid endoscope telescope.

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 cea0a21a-373f-43e3-9089-80de2fd7e90f 35 fields · synced Jun 1, 2026