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Kendall

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Kendall FDA UDI
Generic Name
Surgical scrub brush, reusable FDA UDI
Device Name
Sponge Stick with PVP-I FDA UDI
Model / Reference
41550 FDA UDI
Description
Sponge Stick with PVP-I FDA UDI

Identifiers

Catalog Number
41550 FDA UDI
Primary DI / UDI-DI
10884527018758 FDA UDI
FDA Product Code
GEC FDA UDI
GMDN Term
Surgical scrub brush, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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: Surgical scrub brush, reusable

Kendall by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical scrub brush, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 53ce6688-0b4e-4112-830c-732511d0edf5 36 fields · synced May 30, 2026