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VentriClear

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
VentriClear FDA UDI
Generic Name
Intracerebral infusion/drainage catheter, short-term FDA UDI
Device Name
VentriClear II Ventricular Drainage Catheter FDA UDI
Model / Reference
G44130 FDA UDI
Description
VentriClear II Ventricular Drainage Catheter FDA UDI

Identifiers

Catalog Number
50318 FDA UDI
Primary DI / UDI-DI
00827002441309 FDA UDI
FDA Product Code
NHC FDA UDI
GMDN Term
Intracerebral infusion/drainage catheter, short-term FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4100 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

Category: Intracerebral infusion/drainage catheter, short-term

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

Similar devices

Also classified as Intracerebral infusion/drainage catheter, short-term.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 20478808-d58b-424f-8f62-f0861f80e94f 36 fields · synced Jun 8, 2026