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Sklar®

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar® FDA UDI
Generic Name
Wire cutter FDA UDI
Device Name
CENSITRAC READY MULT ACTION BONE PIN CUT 15 FDA UDI
Model / Reference
40-1715C FDA UDI
Description
CENSITRAC READY MULT ACTION BONE PIN CUT 15 FDA UDI

Identifiers

Primary DI / UDI-DI
10649111441950 FDA UDI
FDA Product Code
HTZ FDA UDI
GMDN Term
Wire cutter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Wire cutter

A comprehensive medical device directory, providing detailed information about the Sklar Wire Cutter. This heavy-duty, hand-held manual surgical instrument is designed to cut orthopaedic wires, cerclages, and small diameter pins or bolts with sturdy handles and blade-like jaws made of high-grade stainless steel.

Similar devices

Also classified as Wire cutter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI 65b92735-29bf-4917-8ca9-076bec43e1e3 33 fields · synced Jul 22, 2026