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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
Rigid endoscope working guide FDA UDI
Device Name
Laser Cysto examination insert w.8Fr. _x000D_working channel _x000D_ FDA UDI
Model / Reference
39.007.50QL FDA UDI
Description
Laser Cysto examination insert w.8Fr. _x000D_working channel _x000D_ FDA UDI

Identifiers

Primary DI / UDI-DI
04050659376212 FDA UDI
FDA Product Code
FDC FDA UDI
GMDN Term
Rigid endoscope working guide 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: Rigid endoscope working guide

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

Similar devices

Also classified as Rigid endoscope working guide.

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 fffc714a-5303-473d-836c-c2d65ba4281d 33 fields · synced May 30, 2026