← Back to catalogue

Gunther Tulip

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Gunther Tulip FDA UDI
Generic Name
Vena cava filter, temporary/permanent FDA UDI
Device Name
Gunther Tulip Vena Cava Filter Set Universal Set FDA UDI
Model / Reference
G21360 FDA UDI
Description
Gunther Tulip Vena Cava Filter Set Universal Set FDA UDI

Identifiers

Catalog Number
IGTCFS-65-UNI FDA UDI
Primary DI / UDI-DI
10827002213606 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

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Vena cava filter, temporary/permanent

Gunther Tulip by Cook Incorporated — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 49cc39a3-995f-4469-b874-5d56b2c9c4cf 36 fields · synced Jun 8, 2026