Leukoplast® 76450-17
Ref 76450-17
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 | Number4042809400329489E 04042809659061 | Date25 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04042809659061 | Date17 Apr 2024 | 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- Withdrawn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
- Leukoplast®
- Generic Name
- Skin-cover adhesive strip, non-antimicrobial
- Device Name
- Leukoplast® soft white
- Model / Ref / Catalog
- 76450-17
- Primary DI / UDI-DI
- 04042809659061
- Basic UDI-DI
- 4042809400329489E
- Unit of Use DI
- 04042809659078
- FDA Product Code
- NAD
- EMDN Code
- M04010101 Non-woven adhesive dressings, with absorbent pad
- GMDN Term
- Skin-cover adhesive strip, non-antimicrobial
- Device Class
- Class I
- Regulation Number
- 878.4020
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 3.8 CentimeterLength — 7.2 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