ALEGRO Alginate
by Alegro Medical GmbH 6 variants
Ref 60001, 61014, 60006, 60008, 60212, 60213, 60002, 61012, 60007, 61011
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberPP00597ALGCFV00142 | Date22 Nov 2022 | StatusActive |
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- Withdrawn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
- Model / Reference
- 60001, 61014, 60006, 60008, 60212, 60213, 60002, 61012, 60007, 61011
- Primary DI / UDI-DI
- 110364512863, 110364532992, 110364518604, 110364520061, 110364527589, 110364528155, 110364513429, 110364530639, 110364519267, 110364529845
- Basic UDI-DI
- PP00597ALGCFV00142
- Unit of Use DI
- 1
- EMDN Code
- M03020299 Medicated bandages, with zinc oxide and other components - other
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000026024
Other devices from Alegro Medical GmbH
Properties
Other properties (13)
- 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