Agremon
by Özden Tip Tibbi̇ Ci̇haz Ve Malzemeler Gida Teksti̇l Ti̇c.ltd.şti̇. 138 variants
Ref DUMBELL-2Model AGREMON
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 | Number868407652AGREMON_01KG 08684076521151 | Date15 Sep 2026 | 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- Withdrawn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
- Reusable Instruments
- Model / Reference
- AGREMON, DUMBELL-2
- Primary DI / UDI-DI
- 08684076521151
- Basic UDI-DI
- 868407652AGREMON_01KG
- EMDN Code
- Y241899 Arm, hand, finger function aid and/or substitution devices - other
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000046965
Other devices from Özden Tip Tibbi̇ Ci̇haz Ve Malzemeler Gida Teksti̇l Ti̇c.ltd.şti̇.
See all devices from Özden Tip Tibbi̇ Ci̇haz Ve Malzemeler Gida Teksti̇l Ti̇c.ltd.şti̇. →
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