Vena Tech

FDA UDI

Class II (US FDA UDI)

by B Braun Interventional Systems, Inc

Identity

Trade Name: VENA TECH FDA UDI
Generic Name: Vena cava filter, permanent FDA UDI
Device Name: VenaTech® Convertible™ FDA UDI
Model / Reference: 5010028 FDA UDI
Description: VenaTech® Convertible™ FDA UDI

Identifiers

Catalog Number: 5010028 FDA UDI
Primary DI / UDI-DI: 04027478130752 FDA UDI
510(k) Number: K152765 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 12.90 French FDA UDI

Category: Vena cava filter, permanent

Vena Tech by B Braun Interventional Systems, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Greenfield™ — Boston Scientific · Class II
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Greenfield™ — Boston Scientific · 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: B Braun Interventional Systems, Inc

Sources (1)

FDA UDI c60c93c2-b64d-4b20-b596-24b1e8740e33 38 fields · synced Jun 6, 2026