Lacing Devices
by Shandong Lianfa Medical Plastic Products Co., Ltd. 5 variants
Ref LF/CE-01Model LDA; LDC; LDE; LDF; LDC-Ⅱ; LDE-Ⅱ; LDF-Ⅱ
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 | Number694951701VA | Date3 Jun 2024 | 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- Withdrawn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
- Lacing Devices
- Model / Reference
- LDA, LDC, LDE, LDF, LDC-Ⅱ, LDE-Ⅱ, LDF-Ⅱ, LF/CE-01
- Primary DI / UDI-DI
- 06949517009110, 06949517009851
- Basic UDI-DI
- 694951701VA
- EMDN Code
- V9099 Various devices not included in other classes - other
- Device Class
- Class I
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- CN-MF-000028790
- Authorised representative
- Linkfar Healthcare GmbH DE-AR-000005107
Other devices from Shandong Lianfa Medical Plastic Products Co., Ltd.
See all devices from Shandong Lianfa Medical Plastic Products Co., Ltd. →
Properties
Other properties (12)
- Sterile: No
- Implantable: 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