← Back to catalogue

Leukotape

FDA UDI

Class I (US FDA UDI)

by Bsn Medical (pty) Ltd

Identity

Trade Name
Leukotape FDA UDI
Generic Name
Dressing-fixation skin adhesive tape, non-silicone FDA UDI
Device Name
LEUKOTAPE 3.8CMX13.7M TAN 1 P MICRO SERRATED FDA UDI
Model / Reference
76168-00 FDA UDI
Description
LEUKOTAPE 3.8CMX13.7M TAN 1 P MICRO SERRATED FDA UDI

Identifiers

Catalog Number
76168-00 FDA UDI
Primary DI / UDI-DI
04042809042191 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Dressing-fixation skin adhesive tape, non-silicone 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Dimensions & Sizes

Size
Width — 3.8 Centimeter FDA UDI
Length — 1370 Centimeter FDA UDI

Category: Dressing-fixation skin adhesive tape, non-silicone

Leukotape by Bsn Medical (pty) Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dressing-fixation skin adhesive tape, non-silicone.

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 9ca85828-b589-4968-aca9-a7ffdeffaf9e 36 fields · synced Jun 8, 2026