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-coring punch, reusable FDA UDI
Device Name: Zlider SPURLING RONGEUR BL 4.0 x 10.0 mm 190 mm upwards FDA UDI
Model / Reference: 250-731-194 FDA UDI
Description: Zlider SPURLING RONGEUR BL 4.0 x 10.0 mm 190 mm upwards FDA UDI

Identifiers

Catalog Number: 250-731-194 FDA UDI
Primary DI / UDI-DI: 04049197533485 FDA UDI
FDA Product Code: EMH FDA UDI
GMDN Term: Bone-coring punch, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 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-coring punch, reusable

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 60f7eac7-e040-4acd-bbf7-f49ff1e236e2 35 fields · synced May 30, 2026