Innomed
by Zhejiang Longterm Medical Technology Co., Ltd. 192 variants
Ref 5059Model G1302
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number69263655200017Q | Date7 Jul 2022 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Hydrocolloid dressingHydrocolloid blister plaster
- Model / Reference
- G1302, 5059
- Primary DI / UDI-DI
- 06926365561472, 06926365582361
- Basic UDI-DI
- 69263655200017Q, 69263655200057Y
- Direct Marketing DI
- 0692636556147206926365582361
- EMDN Code
- M04040301 Hydrocolloid dressings, non-combined
- Device Class
- Class IIbClass IIa
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- CN-MF-000001161
- Authorised representative
- Lotus NL B.V. NL-AR-000000121
Other devices from Zhejiang Longterm Medical Technology Co., Ltd.
See all devices from Zhejiang Longterm Medical Technology Co., Ltd. →
Properties
Other properties (12)
- 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