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PointerTube Kennedy
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref E 01 2108Model Cube 4D Navigation System
by Fiagon GmbH
Identity
- Trade Name
- PointerTube Kennedy EUDAMEDFDA UDI
- Generic Name
- Multi-purpose stereotactic surgery system FDA UDI
- Device Name
- The device PointerTube Kennedy is a navigation probe with suction function for image guided surgery. The device is component to the Cube4D Navigation system. FDA UDI
- Model / Reference
- Cube 4D Navigation System EUDAMEDE 01 2108 EUDAMEDE012108 FDA UDI
- Description
- The device PointerTube Kennedy is a navigation probe with suction function for image guided surgery. The device is component to the Cube4D Navigation system. FDA UDI
Identifiers
- Catalog Number
- E012108 FDA UDI
- Primary DI / UDI-DI
- 04260759930355 EUDAMEDFDA UDI
- Basic UDI-DI
- 426075993E1006C EUDAMED
- Direct Marketing DI
- 04260759930355 EUDAMED
- 510(k) Number
- K163416 FDA UDI
- FDA Product Code
- PGW FDA UDI
- EMDN Code
- Z12011401 SURGICAL NAVIGATION SYSTEM EUDAMED
- GMDN Term
- Multi-purpose stereotactic surgery system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 882.4560 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
PointerTube Kennedy by Fiagon GmbH — 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 | 426075993E1006C | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Fiagon GmbH
- EUDAMED SRN
- DE-MF-000010763
Sources (2)
- EUDAMED 7e6e5cfc-a0bc-4176-9c2e-e4b6fa3ae4b1 61 fields · synced Jun 19, 2026
- FDA UDI 2bb95319-3be9-4f7d-90e8-a1fed8fa392c 36 fields · synced May 30, 2026