Flowertip
by Chetan Meditech Pvt. Ltd. 13 variants
Part of a family of 185 devices: see the family page
Ref BAK-7045.60Model Measurable Arthroscopy and Orthopaedic Instruments
Flowertip (BAK-7045.60) is a Class I device made by Chetan Meditech Pvt. Ltd., registered in EUDAMED on 25 Apr 2025 (Basic UDI-DI 89042103cmplins003YB) with CE/MDR certificate 2024-MDR/QS-040 valid until 1 Jul 2029, active as of 22 Oct 2026.
Active
CE MDR
Valid until
1 Jul 2029
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number89042103cmplins003YB 18904210397723 | Date25 Apr 2025 | StatusActive |
Official records
- EUDAMED public site 89042103cmplins003YB
Certificates
- 2024-MDR/QS-040 Active
Quality management system EU MDR
- Certifier
- 3EC International a.s. 2265
- Issued
- 1 Jul 2024
- Expires
- 1 Jul 2029
Timeline
- Certificate issued EUDAMED 2024-MDR/QS-040
- Registered EUDAMED 89042103cmplins003YB
- Certificate expires EUDAMED 2024-MDR/QS-040
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- BIOTEK, Cannudrill, Flowertip, AI Reamer, Shuttleferry, Shuttleferry I, sHUTTLEFERRY II, Arthrovims OnLoc
- Model / reference
- Measurable Arthroscopy and Orthopaedic Instruments, BAK-7045.60
- Primary DI / UDI-DI
- 18904210397723
- Basic UDI-DI
- 89042103cmplins003YB
- EMDN code
- L091001, L1999
- 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
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