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VADER Pedicle System, Navigated Cannulated Tap, Ø 7.5 mm
FDA UDIEUDAMEDClass II (US FDA UDI)
by Icotec
Identity
- Trade Name
- VADER Pedicle System, Navigated Cannulated Tap, Ø 7.5 mm FDA UDI
- Generic Name
- Bone tap, reusable FDA UDI
- Device Name
- VADER Pedicle System, Navigated Cannulated Tap, Ø 7.5 mm FDA UDI
- Model / Reference
- 42-641N FDA UDI
- Description
- VADER Pedicle System, Navigated Cannulated Tap, Ø 7.5 mm FDA UDI
Identifiers
- Catalog Number
- 42-641N FDA UDI
- Primary DI / UDI-DI
- 07640172552384 FDA UDI
- FDA Product Code
- OLO FDA UDI
- GMDN Term
- Bone tap, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Category: Bone tap, reusable
VADER Pedicle System, Navigated Cannulated Tap, Ø 7.5 mm by Icotec — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Bone tap, reusable.
- BIOSURE — Smith & Nephew, Inc. · Class I
- NobelActive® — Nobel Biocare AG · Class I
- CORTICAL TAP — Biomet Orthopedics, Inc. · Class I
- PressON™ — NEXUS SPINE, L.L.C. · Class I
- Insite — TORNIER, INC. · Class I
- ReLine — Nuvasive, Inc. · Class I
- Mariner MIS — SeaSpine Orthopedics Corporation · Class I
- Response 5.5/6.0 Spine System — ORTHOPEDIATRICS CORP. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class II | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Icotec
Sources (2)
- FDA UDI 850e425f-9c5f-4dce-9eed-e8e8d0b8563a 35 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 4, 2026