Canwell
by Canwell Medical Co., Ltd. 1,000+ variants
Part of a family of 217 devices: see the family page
Ref 213410018
Canwell (213410018) is a Class I device made by Canwell Medical Co., Ltd, registered in EUDAMED on 9 Jan 2026 (Basic UDI-DI 69429802KH0010GC) with CE/MDR certificate 6142788CE01 valid until 1 Mar 2029, active as of 23 Oct 2026.
Active
CE MDR
Valid until
1 Mar 2029
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number6142788CE01 | Date26 May 2026 | StatusActive |
Official records
- EUDAMED public site 69429802KH0010GC
Certificates
- 6142788CE01 Active
Quality assurance EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 26 May 2026
- Expires
- 1 Mar 2029
- Reason
- Ar data change
Timeline
- Registered EUDAMED 69429802KH0010GC
- Certificate issued EUDAMED 6142788CE01
- Certificate expires EUDAMED 6142788CE01
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Orthopedic Instruments (BONE SPOONS)
- Model / reference
- 213410018
- Primary DI / UDI-DI
- 06942980291884
- Basic UDI-DI
- 69429802KH0010GC
- EMDN code
- L0901 Orthopaedic surgery spoons and curettes, reusable
- Device class
- Class I
- EU registration type
- Standard device
Manufacturer details
- EUDAMED SRN
- CN-MF-000025329
- Authorised representative
- Llins Service & Consulting GmbH DE-AR-000009077
Similar devices in this category
Other devices filed under ORTHOPAEDIC SURGERY SPOONS AND CURETTES, REUSABLE.