Elastus HydroZink
by Alegro Medical GmbH 3 variants
Ref 71026 / 60021, 71025 / 60022, 71023 / 60023, 71024 / 60024
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- Withdrawn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
- Device Name
- ALEGRO Alginate
- Model / Reference
- 71026 / 60021, 71025 / 60022, 71023 / 60023, 71024 / 60024
- Primary DI / UDI-DI
- 04260585132213, 04260585132220, 04260585132237, 04260585132244
- Basic UDI-DI
- PP00597ALGCFV00142
- Direct Marketing DI
- 04260585132213042605851322200426058513223704260585132244
- 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