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Scissors

FDA UDI

Class I (US FDA UDI)

by Dr.frigz International(pvt)ltd,

Identity

Trade Name
SCISSORS FDA UDI
Generic Name
Bandage scissors, single-use FDA UDI
Device Name
LISTER BANDAGE SCISSORS 7" FDA UDI
Model / Reference
LISTER BANDAGE SCISSORS FDA UDI
Description
LISTER BANDAGE SCISSORS 7" FDA UDI

Identifiers

Catalog Number
LBS7PAS FDA UDI
Primary DI / UDI-DI
B974LBS7PAS0 FDA UDI
FDA Product Code
JOK FDA UDI
GMDN Term
Bandage scissors, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 7 Inch FDA UDI

Category: Bandage scissors, single-use

Scissors by Dr.frigz International(pvt)ltd, — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bandage scissors, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d2f69ec5-13d2-4082-83bd-4eede5eb9113 35 fields · synced May 30, 2026