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Cook

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Cook FDA UDI
Generic Name
Gastro-urological guidewire, single-use FDA UDI
Device Name
Wire Guide With 1cm Flexible Tip FDA UDI
Model / Reference
G14471 FDA UDI
Description
Wire Guide With 1cm Flexible Tip FDA UDI

Identifiers

Catalog Number
638421 FDA UDI
Primary DI / UDI-DI
00827002144712 FDA UDI
FDA Product Code
OCY FDA UDI
GMDN Term
Gastro-urological guidewire, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Cook by Cook Incorporated — 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

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI ed0ba001-0557-4b96-b57d-bbf99e4e2775 37 fields · synced Jun 8, 2026