Viscoplast™ Max Hold
by 3M Company
Ref V5D28W12N
Viscoplast™ Max Hold (V5D28W12N) is a Class I device made by 3M Company, registered in EUDAMED on 7 Apr 2026 (Basic UDI-DI 06082238401050000000008E6), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number06082238401050000000008E6 04054596753990 | Date7 Apr 2026 | StatusActive |
Official records
- EUDAMED public site 06082238401050000000008E6
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- Withdrawn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 — CE/MDR Active
Specification
- Device name
- Nexcare™ Max Hold Waterproof Bandages
- Model / reference
- V5D28W12N
- Primary DI / UDI-DI
- 04054596753990
- Basic UDI-DI
- 06082238401050000000008E6
- EMDN code
- M04010102 Polyurethane (or other material) adhesive dressings, with absorbent pad
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- US-MF-000014086
- Authorised representative
- 3M Deutschland GmbH (Medical) DE-AR-000011642
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