Neurotupfer
by HGV - Verbandstoffe Gesellschaft mit beschränkter Haftung
Ref 634001
Active
CE MDR
Valid until
3 Dec 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number++B819NeurotupferM3 +B8196340011 | Date23 Feb 2026 | StatusActive |
Certificates
- 44911220468 Active
Quality management system EU MDR
- Certifier
- TÜV NORD CERT GmbH 0044
- Issued
- 4 Dec 2025
- Expires
- 3 Dec 2030
- 44912220468 Active
Technical documentation EU MDR
- Certifier
- TÜV NORD CERT GmbH 0044
- Issued
- 4 Dec 2025
- Expires
- 3 Dec 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Neurotupfer
- Model / Reference
- 634001
- Primary DI / UDI-DI
- +B8196340011
- Basic UDI-DI
- ++B819NeurotupferM3
- EMDN Code
- M0202030101 Non-woven gauze pads, without x-ray detectable thread, sterile
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000007886
Other devices from HGV - Verbandstoffe Gesellschaft mit beschränkter Haftung
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