Solidea 067726
Part of a family of 2,253+ devices: see the family page
Ref 060470
Solidea 067726 (060470) is a Class I device made by Calzificio Pinelli SRL, registered in EUDAMED on 5 May 2026 (Basic UDI-DI 83004960079DC23) and listed in FDA GUDID since 2 Nov 2023 (UDI-DI 08300496067726), active as of 23 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number83004960079DC23 08300496067726 | Date5 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08300496067726 | Date2 Nov 2023 | StatusListed |
Official records
- EUDAMED public site 83004960079DC23
- AccessGUDID record 08300496067726
Across registries
- EUDAMED Basic UDI-DI 83004960079DC23 registered 5 May 2026 Active
- FDA GUDID UDI-DI 08300496067726 listed 2 Nov 2023 Listed
Timeline
- Listed FDA GUDID 08300496067726
- Registered EUDAMED 83004960079DC23
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Essentia Bamboo Gladys EUDAMEDSolidea GUDID
- Generic name
- Compression/pressure sock/stocking, reusable
- Device name
- Preventive Line
- Model / Ref / Catalog
- 060470, 067726
- Primary DI / UDI-DI
- 08300496067726
- Basic UDI-DI
- 83004960079DC23
- FDA product code
- FQL
- EMDN code
- M030499 Elastic bandages, support and compression - other
- GMDN term
- Compression/pressure sock/stocking, reusable
- Device class
- Class I
- Regulation number
- 880.5780
- EU registration type
- Standard device
- EU market of registration
- Italy
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 060470 | 067726 |
Similar devices in this category
Other devices filed under ELASTIC BANDAGES, SUPPORT AND COMPRESSION.