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Mckesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
Mckesson FDA UDI
Generic Name
Bandage scissors, reusable FDA UDI
Device Name
SCISSOR, BANDAGE LISTER SUPERC FDA UDI
Model / Reference
43-1-243 FDA UDI
Description
SCISSOR, BANDAGE LISTER SUPERC FDA UDI

Identifiers

Primary DI / UDI-DI
00612479239593 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Bandage 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bandage scissors, reusable

Mckesson Bandage Scissors, a highly effective and versatile surgical instrument designed for cutting bandages and cloth. Utilizing two pivoted blades with finger and thumb holes in the handles, this device is engineered to provide precise cuts while ensuring user safety.

Similar devices

Also classified as Bandage scissors, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mckesson Medical-Surgical Inc.

Sources (1)

  • FDA UDI 987b5b44-a79a-4b19-ace0-ae6b57db4b7b 33 fields · synced Jul 23, 2026