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Tensoplast

FDA UDI

Class I (US FDA UDI)

by Bsn Medical (pty) Ltd

Identity

Trade Name
Tensoplast FDA UDI
Generic Name
Pressure bandage, non-latex, reusable FDA UDI
Device Name
TENSOPLAST 10CM X 4.5M 1 B 1CT/12 BEA S FDA UDI
Model / Reference
72050-42 FDA UDI
Description
TENSOPLAST 10CM X 4.5M 1 B 1CT/12 BEA S FDA UDI

Identifiers

Catalog Number
72050-42 FDA UDI
Primary DI / UDI-DI
04042809018707 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Pressure bandage, non-latex, reusable 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

Yes

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
Length — 450 Centimeter FDA UDI
Width — 10 Centimeter FDA UDI

Category: Pressure bandage, non-latex, reusable

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

Similar devices

Also classified as Pressure bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d47c2b4d-5599-4a5c-bb2a-380ea2b39cbe 36 fields · synced Jun 6, 2026