iFIT Prosthesis
by iFIT Prosthetics 12 variants
Ref TT200RiModel TT200
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number0850049686TT200i64 00850049686167 | Date15 Mar 2023 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- International KIT - Transtibial prosthetic device
- Model / Reference
- TT200, TT200Ri
- Primary DI / UDI-DI
- 00850049686167
- Basic UDI-DI
- 0850049686TT200i64
- Direct Marketing DI
- 00850049686167
- EMDN Code
- Y062409 Transtibial prostheses (for amputation under knee)
- Device Class
- Class I
- EU market of registration
- Northern Ireland
Manufacturer details
- EUDAMED SRN
- US-MF-000032928
- Authorised representative
- Eurolink Europe Compliance Limited IE-AR-000002852
Other devices from iFIT Prosthetics
Properties
Other properties (13)
- 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
- Measuring Function: No
- Incorporates Medicinal Product: No