Identity
- Trade Name
- Actimove FDA UDI
- Generic Name
- Pressure bandage, Hevea-latex, single-use FDA UDI
- Device Name
- ACTIMOVE ELASTIKON ELASTIC TAPE 2"X2.5YDS PINK / BEIGE 6 (5.1CMX2.2M) FDA UDI
- Model / Reference
- 73080-24 FDA UDI
- Description
- ACTIMOVE ELASTIKON ELASTIC TAPE 2"X2.5YDS PINK / BEIGE 6 (5.1CMX2.2M) FDA UDI
Identifiers
- Catalog Number
- 73080-24 FDA UDI
- Primary DI / UDI-DI
- 04042809819922 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
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
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
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 220 Centimeter FDA UDIWidth — 5.1 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
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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 802b3a8f-d860-485a-8df2-dfc40f8aecf3 37 fields · synced May 30, 2026