Plastic medication box
by Anhui E-link Plastic Industry Co., Ltd 27 variants
Ref EK-389
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 | Number698058443PMB01LZ 06980584430216 | Date28 Sep 2026 | 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- Withdrawn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
- Plastic medication box
- Model / Reference
- EK-389
- Primary DI / UDI-DI
- 06980584430216
- Basic UDI-DI
- 698058443PMB01LZ
- Direct Marketing DI
- 06980584430216
- EMDN Code
- A99 Devices for administration, withdrawal and collection - other
- Device Class
- Class I
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- CN-MF-000059297
- Authorised representative
- Lotus NL B.V. NL-AR-000000121
Other devices from Anhui E-link Plastic Industry Co., Ltd
See all devices from Anhui E-link Plastic Industry Co., Ltd →
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