Identity
- Trade Name
- Denali® Vena Cava Filter FDA UDI
- Generic Name
- Vena cava filter, temporary/permanent FDA UDI
- Device Name
- DENALI® Vena Cava Filter Femoral FDA UDI
- Model / Reference
- DL900F FDA UDI
- Description
- DENALI® Vena Cava Filter Femoral FDA UDI
Identifiers
- Catalog Number
- DL900F FDA UDI
- Primary DI / UDI-DI
- 00801741040801 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Vena cava filter, temporary/permanent
Denali® Vena Cava Filter by Bard Peripheral Vascular — 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
- Bard Peripheral Vascular
Sources (1)
- FDA UDI a4cc6bb4-f747-4ef2-8d37-06262264f1a3 37 fields · synced May 30, 2026