Sklar®

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name: Sklar® FDA UDI
Generic Name: General-purpose surgical scissors, reusable FDA UDI
Device Name: JORGENSON SCISS 20" STRONG CUR FDA UDI
Model / Reference: 61-2011 FDA UDI
Description: JORGENSON SCISS 20" STRONG CUR FDA UDI

Identifiers

Primary DI / UDI-DI: 10649111032080 FDA UDI
FDA Product Code: LRW FDA UDI
GMDN Term: General-purpose surgical scissors, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose surgical scissors, reusable

Sklar® by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
Tecomet — Tecomet,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: Sklar Corporation

Sources (1)

FDA UDI 7c8cd25b-4d06-4c13-8808-b79da6543660 33 fields · synced May 30, 2026