Tukikaide K-28, RST, 800 mm, tukijalka
by Tukimet Oy
Ref 305828HModel 3000
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Overview
Tukikahvat ja -kaiteet, Tukimet Oyin tuotantoon sisältyvät ulkoiluvälineet ovat suurimmasta osin hyödyllisiä terveydentilän hoitoon. Tukikaide on kehitetty ja valmistettu myös luonteenmukaisesti, jotta sen käyttäjille tarjoavat parhaansa mahdolliset hyöty ja riskejä vähentämiseksi.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number6430057233000TE 06430057230152 | Date15 Nov 2021 | 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- Withdrawn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
- Model / Reference
- 3000, 305828H
- Primary DI / UDI-DI
- 06430057230152
- Basic UDI-DI
- 6430057233000TE
- EMDN Code
- Y181803 Handrails
- Device Class
- Class I
- EU market of registration
- Finland
Manufacturer details
- EUDAMED SRN
- FI-MF-000006700
Other devices from Tukimet Oy
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