K-Wire w. double end trocarpoint 1.40mm/152mm, 6 pcs./unit

FDA UDI

Class II (US FDA UDI)

by mahe medical gmbh

Identity

Trade Name: K-Wire w. double end trocarpoint 1.40mm/152mm, 6 pcs./unit FDA UDI
Generic Name: Orthopaedic bone wire FDA UDI
Device Name: K-Wire w. double end trocarpoint 1.40mm/152mm, 6 pcs./unit FDA UDI
Model / Reference: KM71-024 FDA UDI
Description: K-Wire w. double end trocarpoint 1.40mm/152mm, 6 pcs./unit FDA UDI

Identifiers

Catalog Number: KM71-024 FDA UDI
Primary DI / UDI-DI: EMAHKM710240 FDA UDI
FDA Product Code: HTY FDA UDI
GMDN Term: Orthopaedic bone wire FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 1.40 Millimeter FDA UDI
Length — 152 Millimeter FDA UDI

Category: Orthopaedic bone wire

K-Wire w. double end trocarpoint 1.40mm/152mm, 6 pcs./unit by mahe medical gmbh — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: mahe medical gmbh

Sources (1)

FDA UDI 788eb5cd-a49e-4611-82a2-a29a39021b68 36 fields · synced Jun 8, 2026