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Fentex

FDA UDI

Class I (US FDA UDI)

by FENTEX medical GmbH

Identity

Trade Name
FENTEX FDA UDI
Generic Name
Tuning fork FDA UDI
Device Name
Tuning Fork by Hartmann with clamps, C = 64 Hz FDA UDI
Model / Reference
038310FX FDA UDI
Description
Tuning Fork by Hartmann with clamps, C = 64 Hz FDA UDI

Identifiers

Catalog Number
038310FX FDA UDI
Primary DI / UDI-DI
04250407703981 FDA UDI
FDA Product Code
GWX FDA UDI
GMDN Term
Tuning fork FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.1525 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: Tuning fork

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

Similar devices

Also classified as Tuning fork.

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 e1ef6c3a-9720-42a4-b1ad-959e3b415286 35 fields · synced May 30, 2026