Chiroklip wire protector 2 pack blister/box with 25 blisters

FDA UDI

Class I (US FDA UDI)

by Osteotec, Ltd.

Identity

Trade Name: Chiroklip wire protector 2 pack blister/box with 25 blisters FDA UDI
Generic Name: Orthopaedic bone pin cover FDA UDI
Device Name: ChiroKlip is a small butterfly shaped aluminium clip with an adhesive foam covering. It is designed to fold around the end of a K wire and to safely protect the wearer from the risk of injury or re-injury through catching the sharp end of the K wire on clothing, bedclothes, people or other objects. Each Chiroklip box contain 25 Chiroklip pairs FDA UDI
Model / Reference: CKB2 FDA UDI
Description: ChiroKlip is a small butterfly shaped aluminium clip with an adhesive foam covering. It is designed to fold around the end of a K wire and to safely protect the wearer from the risk of injury or re-injury through catching the sharp end of the K wire on clothing, bedclothes, people or other objects. Each Chiroklip box contain 25 Chiroklip pairs FDA UDI

Identifiers

Catalog Number: CKB2 FDA UDI
Primary DI / UDI-DI: 05060079820355 FDA UDI
FDA Product Code: HXQ FDA UDI
GMDN Term: Orthopaedic bone pin cover 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

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Contains Latex

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Prescription Use

FDA UDI

Over-the-Counter

Yes

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Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

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Lot / Batch Number

Yes

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Serial Number

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Expiration Date

Yes

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Manufacturing Date

FDA UDI

Category: Orthopaedic bone pin cover

Chiroklip wire protector 2 pack blister/box with 25 blisters by Osteotec, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin cover.

WishBone K - Wire System — WISHBONE MEDICAL INC. · Class I
WishBone K - Wire System — WISHBONE MEDICAL INC. · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Osteotec, Ltd.

Sources (1)

FDA UDI 3116cac3-eccb-452a-bbda-ce2007ddd010 34 fields · synced Jun 6, 2026