Hermann Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by Hermann Medizintechnik GmbH

Identity

Trade Name: Hermann Medizintechnik GmbH FDA UDI
Generic Name: Suturing needle holder, reusable FDA UDI
Device Name: CASTROVIEJO suturing forceps 10,5cm1x2 teeth, with tying platform,tip 0,3mm FDA UDI
Model / Reference: H143-14903 FDA UDI
Description: CASTROVIEJO suturing forceps 10,5cm1x2 teeth, with tying platform,tip 0,3mm FDA UDI

Identifiers

Primary DI / UDI-DI: 04059453117953 FDA UDI
FDA Product Code: GEN FDA UDI
GMDN Term: Suturing needle holder, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Suturing needle holder, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Hermann Medizintechnik GmbH

Sources (1)

FDA UDI cc046158-9831-48af-840d-7b71ddbe7d32 33 fields · synced Jun 1, 2026