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Scrub Care Exidine

FDA UDI

Class I (US FDA UDI)

by Carefusion 2200, Inc

Identity

Trade Name
Scrub Care Exidine FDA UDI
Generic Name
Surgical patient preparation kit FDA UDI
Device Name
Scrub Care Exidine-4 CHG 4%, Chlorhexidine Gluconate 4% Solution FDA UDI
Model / Reference
CLEAN1 FDA UDI
Description
Scrub Care Exidine-4 CHG 4%, Chlorhexidine Gluconate 4% Solution FDA UDI

Identifiers

Catalog Number
CLEAN1 FDA UDI
Primary DI / UDI-DI
10885403192821 FDA UDI
FDA Product Code
OJU FDA UDI
GMDN Term
Surgical patient preparation kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Convenience Kit

Yes

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

Scrub Care Exidine by Carefusion 2200, Inc — Class I — 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

Sources (1)

  • FDA UDI 957ebea9-29e3-443c-a638-8a34ba78e733 37 fields · synced Jun 8, 2026