RZ Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name: RZ Medizintechnik GmbH FDA UDI
Generic Name: Bone distraction forceps FDA UDI
Device Name: Bankart Perforating Forceps lightly curved, 170mm, 6 3/4'' FDA UDI
Model / Reference: 259-900-000 FDA UDI
Description: Bankart Perforating Forceps lightly curved, 170mm, 6 3/4'' FDA UDI

Identifiers

Catalog Number: 259-900-000 FDA UDI
Primary DI / UDI-DI: 04049197455008 FDA UDI
FDA Product Code: GEN FDA UDI
GMDN Term: Bone distraction forceps 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: Bone distraction forceps

RZ Medizintechnik GmbH by RZ-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: RZ-Medizintechnik GmbH

Sources (1)

FDA UDI b64a7543-2c76-4846-9b57-84952e96c6a4 35 fields · synced May 30, 2026