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Sklar

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar FDA UDI
Generic Name
Rectal scissors FDA UDI
Device Name
LLOYD DAVIS REC SCISS STR10.5 INCHES FDA UDI
Model / Reference
80-1595 FDA UDI
Description
LLOYD DAVIS REC SCISS STR10.5 INCHES FDA UDI

Identifiers

Primary DI / UDI-DI
10649111456794 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Rectal scissors 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: Rectal scissors

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

Similar devices

Also classified as Rectal scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI 9f48993b-1078-4de2-91dc-a9f964f1f68e 33 fields · synced May 31, 2026