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Sign in to claim this brandBSN MEDICAL (PTY) LTD
US
Last updated May 27, 2026
What BSN MEDICAL (PTY) LTD makes
BSN Medical produces pressure bandages, including single-use versions made with Hevea-latex and reusable non-latex types, as well as non-silicone skin adhesive tapes for dressing fixation. Their product line also includes adhesive tapes for medical and sports applications, such as Leukotape and Tensosport, alongside reusable pressure bandages like Actimove and Tensoplast.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) system. The company operates from the United States, adhering to applicable regulatory standards for medical devices in that jurisdiction.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does BSN Medical (PTY) Ltd manufacture?
BSN Medical (PTY) Ltd specializes in pressure bandages and dressing-fixation skin adhesive tapes. Their product line includes single-use pressure bandages made with Hevea-latex, reusable non-latex pressure bandages, and non-silicone adhesive tapes for medical and sports applications, such as Leukotape and Tensosport. These devices are designed for wound care and immobilization purposes.
Where is BSN Medical (PTY) Ltd based?
BSN Medical (PTY) Ltd operates from the United States. The company develops and manufactures its devices in compliance with the regulatory standards applicable to medical devices in that country.
Which regulatory registries list BSN Medical’s devices?
BSN Medical’s devices are listed in the FDA’s Unique Device Identification (UDI) system. This registry ensures traceability and identification of medical devices under FDA regulations, helping to track specific products like Actimove, Tensoplast, and Leukotape.
How are BSN Medical’s devices classified under FDA regulations?
BSN Medical’s devices fall under Class I classification according to FDA regulations. This classification typically applies to low-risk medical devices, such as pressure bandages and adhesive tapes, which pose minimal risk to patients when used as intended. Classification determines the regulatory pathway for authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- essity.com
- —
- —
- [email protected]
- Phone
- +1(800)537-1063
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 636017233
Catalogue (15)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Actimove | 73080-21 | FDA UDI | Class I | Active |
| Tensoplast | 72052-18 | FDA UDI | Class I | Active |
| Actimove | 73080-23 | FDA UDI | Class I | Active |
| Leukotape | 76168-00 | FDA UDI | Class I | Active |
| Tensosport | 72050-15 | FDA UDI | Class I | Active |
| Tensoplast | 72050-43 | FDA UDI | Class I | Active |
| Actimove | 73080-14 | FDA UDI | Class I | Active |
| Actimove | 73080-24 | FDA UDI | Class I | Active |
| Actimove | 73080-22 | FDA UDI | Class I | Active |
| Tensoplast | 72050-42 | FDA UDI | Class I | Active |
| Actimove | 73080-13 | FDA UDI | Class I | Active |
| Actimove | 73080-10 | FDA UDI | Class I | Active |
| Actimove | 73080-19 | FDA UDI | Class I | Active |
| Actimove | 73080-20 | FDA UDI | Class I | Active |
| Tensoplast | 72050-57 | FDA UDI | Class I | Active |
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