Biotek
by Chetan Meditech Pvt. Ltd. 296 variants
Ref 10042Model Reusable Arthroscopy and Orthopaedic Instruments
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 | Number89042103cmplins002Y9 18904210397082 | Date24 Apr 2025 | 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- Withdrawn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
- BIOTEK, Cannudrill, Flowertip, AL Reamer, BOTS, BOATS, SURESHOT, LOCUS, Shuttleferry, Shuttleferry I, Shuttleferry II, Arthrovims, OnLoc
- Model / Reference
- Reusable Arthroscopy and Orthopaedic Instruments, 10042
- Primary DI / UDI-DI
- 18904210397082
- Basic UDI-DI
- 89042103cmplins002Y9
- EMDN Code
- L091001, L1999
- Device Class
- Class I
- EU market of registration
- Greece
Manufacturer details
- EUDAMED SRN
- IN-MF-000013541
- Authorised representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Other devices from Chetan Meditech Pvt. 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