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mahe medical GmbH

FDA UDI

Class I (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
HIGH-FLOW Arthroscopy trocar sheath, _x000D_OD6.5mm,w.2 rotatable stopcock,f.optic _x000D_4.0/176mm/univ. FDA UDI
Model / Reference
50.032.05 FDA UDI
Description
HIGH-FLOW Arthroscopy trocar sheath, _x000D_OD6.5mm,w.2 rotatable stopcock,f.optic _x000D_4.0/176mm/univ. FDA UDI

Identifiers

Primary DI / UDI-DI
04050659387843 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Rigid endoscope working guide FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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 I — 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 dd2832a3-d5b4-4aaa-bc5b-68bf67a89128 33 fields · synced May 30, 2026