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Cook

FDA UDI

Class I (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Cook FDA UDI
Generic Name
Urethral dilatation catheter, non-medicated FDA UDI
Device Name
Malleable Tip Filiform FDA UDI
Model / Reference
G14477 FDA UDI
Description
Malleable Tip Filiform FDA UDI

Identifiers

Catalog Number
110245 FDA UDI
Primary DI / UDI-DI
00827002144774 FDA UDI
FDA Product Code
FBW FDA UDI
GMDN Term
Urethral dilatation catheter, non-medicated FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5520 FDA UDI
Commercial Distribution
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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Urethral dilatation catheter, non-medicated

Cook by Cook Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urethral dilatation catheter, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI fe149a1f-5c11-4a37-8157-f3d2e975df64 36 fields · synced Jun 8, 2026