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Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Flexible endoscopic cytology brush, single-use FDA UDI
Device Name
Cardinal Health; Endo Valve Brush; Dual Ended Valve Brush; Variable Brush Head Sizes Fit All Buttons and Valves FDA UDI
Model / Reference
G4VB FDA UDI
Description
Cardinal Health; Endo Valve Brush; Dual Ended Valve Brush; Variable Brush Head Sizes Fit All Buttons and Valves FDA UDI

Identifiers

Catalog Number
G4VB FDA UDI
Primary DI / UDI-DI
10885380070402 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Flexible endoscopic cytology brush, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Category: Flexible endoscopic cytology brush, single-use

Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic cytology brush, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 644da3e9-29ac-44a2-9d86-1496805649ae 34 fields · synced Jun 8, 2026