Kula łokciowa Niebieska AXIS ERGO
Ref OG-MO-AXI -ERG-BLU-UN
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Overview
Meet Kula łokciowa Niebieska AXIS ERGO, a highly effective and reliable orthopedic device designed for the prevention and treatment of orthopedic conditions. Our innovative product features cutting-edge technology and improved patient outcomes. Learn more about its key benefits, regulatory compliance, and FAQs.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number5905957672OG-MO-AXI-ERG6Z 05905957672292 | Date23 Apr 2026 | 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- Withdrawn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
- OG-MO-AXI -ERG-BLU-UN
- Primary DI / UDI-DI
- 05905957672292
- Basic UDI-DI
- 5905957672OG-MO-AXI-ERG6Z
- Direct Marketing DI
- 05905957672292
- EMDN Code
- Y12030601 Elbow crutches
- Device Class
- Class I
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- PL-MF-000050865
Other devices from Orthoguard Sp. z o.o.
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