← Back to catalogue

RZ Medizintechnik GmbH

FDA UDI

Class I (US FDA UDI)

by RZ-Medizintechnik GmbH

Identity

Trade Name
RZ Medizintechnik GmbH FDA UDI
Generic Name
Tongue depressor, surgical FDA UDI
Device Name
Stierlen Tongue Depressor 55mm FDA UDI
Model / Reference
430-350-005 FDA UDI
Description
Stierlen Tongue Depressor 55mm FDA UDI

Identifiers

Catalog Number
430-350-005 FDA UDI
Primary DI / UDI-DI
04049197477659 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Tongue depressor, surgical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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: Tongue depressor, surgical

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

Similar devices

Also classified as Tongue depressor, surgical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e181d755-8685-44fb-abca-f8f59a6e7a13 35 fields · synced May 31, 2026