Tubifast® 2436
Ref 2436
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number07333350016487 | Date15 Sep 2026 | StatusListed |
| European Union | CE/MDR EUDAMED | Number733243000000000064K2 07333350016487 | Date9 Sep 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Tubifast EUDAMEDTubifast® GUDID
- Generic Name
- Tubular support bandage, non-latex, reusable
- Model / Reference
- 2436
- Primary DI / UDI-DI
- 07333350016487
- Basic UDI-DI
- 733243000000000064K2
- FDA Product Code
- FQM
- EMDN Code
- M0303010103 Elastic fixing bandages, non-adhesive, extensible in two directions
- GMDN Term
- Tubular support bandage, non-latex, reusable
- Device Class
- Class I
- Regulation Number
- 880.5075
- EU market of registration
- Sweden
- GUDID distribution status
- In Commercial Distribution
Other devices from Mölnlycke Health Care AB
Properties
Other properties (21)
- Sterile: No
- Single Use: 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
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No