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Cook

FDA UDI

Class III (US FDA UDI)

by William A. Cook Australia Pty. Ltd.

Identity

Trade Name
COOK FDA UDI
Generic Name
Synthetic vascular graft FDA UDI
Device Name
Zenith Iliac Branch FDA UDI
Model / Reference
G60347 FDA UDI
Description
Zenith Iliac Branch FDA UDI

Identifiers

Catalog Number
ZBIS-12-61-58-US FDA UDI
Primary DI / UDI-DI
00827002603479 FDA UDI
PMA Number
P020018 FDA UDI
FDA Product Code
MIH FDA UDI
GMDN Term
Synthetic vascular graft FDA UDI

Classification

Device Class
Class III 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: Synthetic vascular graft

Cook by William A. Cook Australia Pty. Ltd. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic vascular graft.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f846213e-403c-4340-81d1-1bd773e97bf5 37 fields · synced Jun 6, 2026