RZ Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name: RZ Medizintechnik GmbH FDA UDI
Generic Name: Rigid endoscopic biopsy forceps, reusable FDA UDI
Device Name: Gruenwald Sinuscopy Forceps 2mm, shaft 70° upwards cvd, left side cutting, WL 130mm, 5 1/8'', with LL FDA UDI
Model / Reference: 252-602-070 FDA UDI
Description: Gruenwald Sinuscopy Forceps 2mm, shaft 70° upwards cvd, left side cutting, WL 130mm, 5 1/8'', with LL FDA UDI

Identifiers

Catalog Number: 252-602-070 FDA UDI
Primary DI / UDI-DI: 04049197450294 FDA UDI
FDA Product Code: GEN FDA UDI
GMDN Term: Rigid endoscopic biopsy forceps, 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

Category: Rigid endoscopic biopsy forceps, 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 bbd59ad0-f6e9-4806-a12e-b5c3c77e28a1 35 fields · synced May 30, 2026