Tensoplast® 76232-01
Ref 76232-01
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number4042809400377519U 04042809468892 | Date31 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04042809468892 | Date8 Dec 2022 | StatusListed |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Tensoplast®
- Generic Name
- Adhesive bandage
- Device Name
- Tensoplast® LF
- Model / Ref / Catalog
- 76232-01
- Primary DI / UDI-DI
- 04042809468892
- Basic UDI-DI
- 4042809400377519U
- Unit of Use DI
- 04042809667868
- FDA Product Code
- KGX
- EMDN Code
- M030402030102 Elastic support bandages, adhesive extensible in one direction, high extensibility
- GMDN Term
- Adhesive bandage
- Device Class
- Class I
- Regulation Number
- 880.5240
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 450 CentimeterWidth — 7.5 Centimeter
Other devices from Bsn Medical, Inc.
Properties
Other properties (19)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Prescription Use: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No