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Denali® Vena Cava Filter

FDA UDI

Class II (US FDA UDI)

by Bard Peripheral Vascular

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
MRI Safety
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

Similar devices

Also classified as Vena cava filter, temporary/permanent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a4cc6bb4-f747-4ef2-8d37-06262264f1a3 37 fields · synced May 30, 2026