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VADER® Pedicle System Screwdriver, Hex, 4 mm
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 42-719Model Screwdriver
by icotec ag
Identity
- Trade Name
- VADER® Pedicle System Screwdriver, Hex, 4 mm EUDAMEDVADER Pedicle System, Screwdriver, Hex, 4 mm FDA UDI
- Generic Name
- Surgical screwdriver, reusable FDA UDI
- Device Name
- VADER Pedicle System, Screwdriver, Hex, 4 mm FDA UDI
- Model / Reference
- Screwdriver EUDAMED42-719 EUDAMEDFDA UDI
- Description
- VADER Pedicle System, Screwdriver, Hex, 4 mm FDA UDI
Identifiers
- Catalog Number
- 42-719 FDA UDI
- Primary DI / UDI-DI
- 07640164844459 EUDAMEDFDA UDI
- Basic UDI-DI
- 764017255iPSI0051B5 EUDAMED
- Direct Marketing DI
- 07640164844459 EUDAMED
- FDA Product Code
- NKB FDA UDI
- EMDN Code
- L1109 NEUROSURGERY AND SPINAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
- GMDN Term
- Surgical screwdriver, reusable FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3070 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
VADER® Pedicle System Screwdriver, Hex, 4 mm by icotec AG — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 764017255iPSI0051B5 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- icotec ag
- EUDAMED SRN
- CH-MF-000026833
- Authorised Representative
- icotec Medical GmbH DE-AR-000016837
Sources (2)
- EUDAMED e11ef740-16e6-4f4d-83ee-d0e11b180e50 61 fields · synced Jul 12, 2026
- FDA UDI 847294fc-5cfb-4585-85be-d164cc3ced33 35 fields · synced May 30, 2026