Actimove

FDA UDI

Class I (US FDA UDI)

by Bsn Medical (pty) Ltd

Identity

Trade Name: Actimove FDA UDI
Generic Name: Pressure bandage, Hevea-latex, single-use FDA UDI
Device Name: ACTIMOVE ELASTIKON ELASTIC TAPE 1"X2.5YDS PINK / BEIGE 12 (2.5CMX2.2M) FDA UDI
Model / Reference: 73080-23 FDA UDI
Description: ACTIMOVE ELASTIKON ELASTIC TAPE 1"X2.5YDS PINK / BEIGE 12 (2.5CMX2.2M) FDA UDI

Identifiers

Catalog Number: 73080-23 FDA UDI
Primary DI / UDI-DI: 04042809819908 FDA UDI
FDA Product Code: KGX FDA UDI
GMDN Term: Pressure bandage, Hevea-latex, single-use 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 220 Centimeter FDA UDI
Width — 2.5 Centimeter FDA UDI

Category: Pressure bandage, Hevea-latex, single-use

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

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Also classified as Pressure bandage, Hevea-latex, single-use.

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Sensi-Wrap, Self Adherent — Dynarex Corp. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Bsn Medical (pty) Ltd

Sources (1)

FDA UDI 5252968c-f505-4142-b3f8-ae537415c5c2 37 fields · synced Jun 1, 2026