Gianturco-Roehm Bird's Nest

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name: Gianturco-Roehm Bird's Nest FDA UDI
Generic Name: Vena cava filter, permanent FDA UDI
Device Name: Gianturco-Roehm Bird's Nest Vena Cava Filter FDA UDI
Model / Reference: G06451 FDA UDI
Description: Gianturco-Roehm Bird's Nest Vena Cava Filter FDA UDI

Identifiers

Catalog Number: BNF-40-PB FDA UDI
Primary DI / UDI-DI: 00827002064515 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

Yes

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

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Vena cava filter, permanent

Gianturco-Roehm Bird's Nest by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Vena cava filter, permanent.

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TrapEase Permanent Vena Cava Filter with the VisEase Angiographic Vessel Dilator — Cordis Corp. · Class II
VENA TECH™ — B BRAUN INTERVENTIONAL SYSTEMS, INC · Class II
Greenfield™ — Boston Scientific · Class II
VENA TECH — B BRAUN INTERVENTIONAL SYSTEMS, INC · 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: Cook Incorporated

Sources (1)

FDA UDI 8580d888-acae-4ac5-ab12-cb5e83498746 36 fields · synced Jun 8, 2026