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Cook Celect

FDA UDI

Class II (US FDA UDI)

by William Cook Europe ApS

Identity

Trade Name
Cook Celect FDA UDI
Generic Name
Vena cava filter, temporary/permanent FDA UDI
Device Name
Cook Celect Platinum, Vena Cava Filter, Femoral and Jugular Approach FDA UDI
Model / Reference
G35580 FDA UDI
Description
Cook Celect Platinum, Vena Cava Filter, Femoral and Jugular Approach FDA UDI

Identifiers

Catalog Number
IGTCFS-65-1-UNI-FT-CELECT-PT FDA UDI
Primary DI / UDI-DI
10827002355801 FDA UDI
510(k) Number
K121629 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
Not 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

Cook Celect by William Cook Europe ApS — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d473abe-c75d-40f4-bb97-f0f9bea10f64 38 fields · synced May 30, 2026