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Hermann Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by Hermann Medizintechnik GmbH

Identity

Trade Name
Hermann Medizintechnik GmbH FDA UDI
Generic Name
Uterine tenaculum FDA UDI
Device Name
ROSEN needle (House-Type), slightly cvdwith round handle, length 16cm, blunt FDA UDI
Model / Reference
H144-71616 FDA UDI
Description
ROSEN needle (House-Type), slightly cvdwith round handle, length 16cm, blunt FDA UDI

Identifiers

Catalog Number
H144-71616 FDA UDI
Primary DI / UDI-DI
04059453124135 FDA UDI
FDA Product Code
GDM FDA UDI
GMDN Term
Uterine tenaculum FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Uterine tenaculum

Hermann Medizintechnik GmbH by Hermann Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Uterine tenaculum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 95af4a0a-d254-4ec6-b416-3669a39cd409 34 fields · synced Jun 8, 2026