VADER® Pedicle System Trial Rod, curved Ø 5.5 mm, R 120, L = 60 mm
EUDAMEDFDA UDIClass IIa (EU MDR)
by icotec ag
Identity
- Trade Name
- VADER® Pedicle System Trial Rod, curved Ø 5.5 mm, R 120, L = 60 mm EUDAMEDVADER Pedicle System Trial Rod, curved Ø 5.5 mm, R 120, L = 60 mm FDA UDI
- Generic Name
- Surgical implant template, reusable FDA UDI
- Device Name
- VADER Pedicle System Trial Rod, curved Ø 5.5 mm, R 120, L = 60 mm FDA UDI
- Model / Reference
- Trial Rod EUDAMED42-910-06 EUDAMEDFDA UDI
- Description
- VADER Pedicle System Trial Rod, curved Ø 5.5 mm, R 120, L = 60 mm FDA UDI
Identifiers
- Catalog Number
- 42-910-06 FDA UDI
- Primary DI / UDI-DI
- 07640164842332 EUDAMEDFDA UDI
- Basic UDI-DI
- 764017255iPSI0055BD EUDAMED
- Direct Marketing DI
- 07640164842332 EUDAMED
- FDA Product Code
- NKB FDA UDI
- EMDN Code
- L1109 NEUROSURGERY AND SPINAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED
- GMDN Term
- Surgical implant template, 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
Single Use
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
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
Yes
Category: Device sterilization/disinfection container, reusable
VADER® Pedicle System Trial Rod, curved Ø 5.5 mm, R 120, L = 60 mm by icotec AG — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 764017255iPSI0055BD | 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 fab3dd7d-dbf8-46c2-ab4d-59c3e3436b1a 61 fields · synced Oct 6, 2026
- FDA UDI 8891a25f-526b-4a09-ae4f-3004b88dd47a 35 fields · synced May 30, 2026