Biotek
by Chetan Meditech Pvt. Ltd. 296 variants
Ref 10697Model Reusable Arthroscopy and Orthopaedic Instruments
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number89042103cmplins002Y9 18904210393879 | 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- Withdrawn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, 10697
- Primary DI / UDI-DI
- 18904210393879
- Basic UDI-DI
- 89042103cmplins002Y9
- EMDN code
- L0919, L1908
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- France
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)
- Supplied sterile: No
- Implantable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No