Venus
by HumanTech Spine GmbH 766 variants
Ref 1005104830
Active
CE MDR
Valid until
11 Feb 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number42505399405ND 04250539913845 | Date29 Sep 2026 | StatusActive |
Certificates
- 1000326894 Active
Quality management system EU MDR
- Certifier
- DQS Medizinprodukte GmbH 0297
- Issued
- 27 Aug 2026
- Expires
- 11 Feb 2031
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- VE Screw
- Model / Reference
- 1005104830
- Primary DI / UDI-DI
- 04250539913845
- Basic UDI-DI
- 42505399405ND
- EMDN Code
- P09070302 Thoracolumbosacral fixation systems
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000010596
Other devices from HumanTech Spine GmbH
Properties
Other properties (12)
- Sterile: 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