← Back to catalogue

Leukostrip™

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew Medical, Ltd.

Identity

Trade Name
LEUKOSTRIP™ FDA UDI
Generic Name
Adhesive bandage FDA UDI
Device Name
Leukostrip S. Wound closure strips. 4mm x 38mm Carton of 50 FDA UDI
Model / Reference
66002882 FDA UDI
Description
Leukostrip S. Wound closure strips. 4mm x 38mm Carton of 50 FDA UDI

Identifiers

Catalog Number
66002882 FDA UDI
Primary DI / UDI-DI
05000223449643 FDA UDI
FDA Product Code
MZR FDA UDI
GMDN Term
Adhesive bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Adhesive bandage

Leukostrip™ by Smith & Nephew Medical, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Adhesive bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI eacd39ff-b058-45cc-bb1b-b9aa5bf41999 34 fields · synced Jun 8, 2026