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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
Orthopaedic bone wire FDA UDI
Device Name
Kirschner w.trocar point,rd.end _x000D_1.6mm/60mm _x000D_ FDA UDI
Model / Reference
004-0331-016 FDA UDI
Description
Kirschner w.trocar point,rd.end _x000D_1.6mm/60mm _x000D_ FDA UDI

Identifiers

Primary DI / UDI-DI
04050659207240 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Orthopaedic bone wire FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Orthopaedic bone wire

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

Similar devices

Also classified as Orthopaedic bone wire.

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 bbca4c2a-6b10-4b2d-b007-d96de1eb3359 33 fields · synced Jun 8, 2026