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RZ Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
RZ Medizintechnik GmbH FDA UDI
Generic Name
ENT soft-tissue cutting forceps FDA UDI
Device Name
Melzer Adenoid Punch Fig. 2 round, with basket, 8mm through cutting 140mm w-l, 5 1/2'' FDA UDI
Model / Reference
420-401-002 FDA UDI
Description
Melzer Adenoid Punch Fig. 2 round, with basket, 8mm through cutting 140mm w-l, 5 1/2'' FDA UDI

Identifiers

Catalog Number
420-401-002 FDA UDI
Primary DI / UDI-DI
04049197474818 FDA UDI
FDA Product Code
KBS FDA UDI
GMDN Term
ENT soft-tissue cutting forceps FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Category: ENT soft-tissue cutting forceps

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

Similar devices

Also classified as ENT soft-tissue cutting forceps.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0d3408d2-f87c-4171-b7a4-bf54ba1463a5 35 fields · synced Jun 8, 2026