Identity
- Trade Name
- Navigator Bionavigation System FDA UDI
- Generic Name
- Intravascular catheter stylet magnet detector FDA UDI
- Device Name
- catheter locating system FDA UDI
- Model / Reference
- 60-3020 FDA UDI
- Description
- catheter locating system FDA UDI
Identifiers
- Catalog Number
- 60-3020 FDA UDI
- Primary DI / UDI-DI
- 10815149025329 FDA UDI
- FDA Product Code
- FOZ FDA UDI
- GMDN Term
- Intravascular catheter stylet magnet detector FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5200 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Intravascular catheter stylet magnet detector
Navigator Bionavigation System by Corpak Medsystems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intravascular catheter stylet magnet detector.
- Sherlock — Bard Access Systems, Inc. · Class II
- Sherlock — Bard Access Systems, Inc. · Class II
- Sherlock — Bard Access Systems, Inc. · Class II
- Navigator — Corpak Medsystems · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Corpak Medsystems
Sources (1)
- FDA UDI 8cc4e9d2-c3cf-4b71-8397-8d585c247a16 35 fields · synced Jun 8, 2026