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LimaCorporate Kirschner wire

FDA UDI

Class II (US FDA UDI)

by Limacorporate

Identity

Trade Name
LimaCorporate Kirschner wire FDA UDI
Generic Name
Orthopaedic intraoperative positioning pin, single-use FDA UDI
Device Name
Dia. 2,5 x 240 mm - K-wire Sterile FDA UDI
Model / Reference
9095.11.953.S FDA UDI
Description
Dia. 2,5 x 240 mm - K-wire Sterile FDA UDI

Identifiers

Catalog Number
9095.11.953.S FDA UDI
Primary DI / UDI-DI
08033390188494 FDA UDI
510(k) Number
K203475 FDA UDI
FDA Product Code
HTY FDA UDI
GMDN Term
Orthopaedic intraoperative positioning pin, single-use 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic intraoperative positioning pin, single-use

LimaCorporate Kirschner wire by Limacorporate — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic intraoperative positioning pin, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI 1a6196a7-c920-4f32-95c2-c8a31850d5f5 36 fields · synced May 30, 2026