Identity
- Trade Name
- Crux® Vena Cava FIlter, Jugular FDA UDI
- Generic Name
- Vena cava filter, temporary/permanent FDA UDI
- Model / Reference
- 7025 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00845225002534 FDA UDI
- FDA Product Code
- DTK FDA UDI
- GMDN Term
- Vena cava filter, temporary/permanent FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.3375 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Vena cava filter, temporary/permanent
Crux® Vena Cava FIlter, Jugular by Volcano Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Volcano Corporation
Sources (1)
- FDA UDI 50fda220-9cdc-413b-a9b3-17df84c0afbb 32 fields · synced Jun 8, 2026