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mahe medical GmbH

FDA UDI

Class II (US FDA UDI)

by mahe medical gmbh

Identity

Trade Name
mahe medical GmbH FDA UDI
Generic Name
Resectoscope FDA UDI
Device Name
Resectoscopy working unit,active, _x000D_closed handle,24/26/28.5Ch _x000D_ FDA UDI
Model / Reference
36.005.02 FDA UDI
Description
Resectoscopy working unit,active, _x000D_closed handle,24/26/28.5Ch _x000D_ FDA UDI

Identifiers

Primary DI / UDI-DI
04050659371484 FDA UDI
FDA Product Code
FDC FDA UDI
GMDN Term
Resectoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Resectoscope

mahe medical GmbH by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resectoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
mahe medical gmbh

Sources (1)

  • FDA UDI 503cca82-b7b7-43b4-9d94-cf1409c52922 33 fields · synced Jun 8, 2026