Multi-parameter detector
by Zhongshan Jinli Electronic Weighing Equipment Co., Ltd. EUDAMED510(k)
Active
Ref KLM-A
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | NumberCN25/00007955 | Date5 Feb 2026 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK231116 | Date15 Jun 2024 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
- CN25/00007955 Issued
Quality management system EU MDR
- Notified body
- Notified body 1639
- Issued
- 5 Feb 2026
- Expires
- 25 Nov 2030
Recalls
No FDA recalls on record, checked 24 Oct 2026.
Specification
- Model / Reference
- KLM-A
- Primary DI / UDI-DI
- 06973337428318
- Basic UDI-DI
- 697333742831L5
- Direct Marketing DI
- 06973337428318
- EMDN Code
- V0399 Measurement devices - other
- Device Class
- Class IIa
- Market of Registration
- Poland
Manufacturer details
- EUDAMED SRN
- CN-MF-000021308
- Authorised representative
- Wellkang Ltd XI-AR-000001836
Other devices from Zhongshan Jinli Electronic Weighing Equipment Co., Ltd.
Properties
Other properties (12)
- 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
- Incorporates Medicinal Product: No