Sklar®

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name: Sklar® FDA UDI
Generic Name: General-purpose surgical scissors, single-use FDA UDI
Device Name: UTILITY SCISS ORNG NS CS50 7" FDA UDI
Model / Reference: 96-5391 FDA UDI
Description: UTILITY SCISS ORNG NS CS50 7" FDA UDI

Identifiers

Primary DI / UDI-DI: 50649111110649 FDA UDI
FDA Product Code: LRW FDA UDI
GMDN Term: General-purpose surgical scissors, single-use 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

Yes

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

Category: General-purpose surgical scissors, single-use

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

Similar devices

Also classified as General-purpose surgical scissors, single-use.

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Surgical Direct — SURGICAL DIRECT, INC. · Class I
Centurion — Centurion Medical Products · Class I
Bioseal Inc. — BIOSEAL · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Surgical Direct — SURGICAL DIRECT, INC. · Class I
Surgical Direct — SURGICAL DIRECT, 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 17705228-5967-435e-bac2-a9a76ed68bb2 33 fields · synced May 30, 2026