Herniatome
Ref 5091945 R
Active
CE MDR
Valid until
15 Jan 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number803373711K0299VX 08053175000407 | Date22 May 2026 | StatusActive |
Certificates
- 0425-MDR-030171-00 Active
Quality management system EU MDR
- Certifier
- ICIM S.P.A. 0425
- Issued
- 16 Jan 2026
- Expires
- 15 Jan 2031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Devices for percutaneous discectomy and motorized for vertebroplasty / kyphoplasty
- Model / Reference
- 5091945 R
- Primary DI / UDI-DI
- 08053175000407
- Basic UDI-DI
- 803373711K0299VX
- EMDN Code
- A01020102 Aspiration fine needles and kits
- Device Class
- Class IIb
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- IT-MF-000027852
Other devices from Adria S.r.l.
Properties
Other properties (12)
- 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