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Vena Tech

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
VENA TECH FDA UDI
Generic Name
Vena cava filter, permanent FDA UDI
Device Name
VENA TECH D-PACK VCF ACCESSORY FDA UDI
Model / Reference
610771 FDA UDI
Description
VENA TECH D-PACK VCF ACCESSORY FDA UDI

Identifiers

Catalog Number
610771 FDA UDI
Primary DI / UDI-DI
04046964332333 FDA UDI
FDA Product Code
DTK FDA UDI
GMDN Term
Vena cava filter, 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

Category: Vena cava filter, permanent

Vena Tech by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vena cava filter, permanent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3befdc6c-4c52-4917-b87d-3815dc4dfe36 35 fields · synced May 30, 2026