Sage

FDA UDI

Class I (US FDA UDI)

by Sage Products Llc

Identity

Trade Name: Sage FDA UDI
Generic Name: Dry medical towel/wipe, single-use FDA UDI
Device Name: Antiseptic Skin Cleansing Kit with 2% Chlorhexidine Gluconate (CHG) FDA UDI
Model / Reference: 9101 FDA UDI
Description: Antiseptic Skin Cleansing Kit with 2% Chlorhexidine Gluconate (CHG) FDA UDI

Identifiers

Catalog Number: 9101 FDA UDI
Primary DI / UDI-DI: 00618029850591 FDA UDI
FDA Product Code: FRL FDA UDI
MAC FDA UDI
GMDN Term: Dry medical towel/wipe, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5300 FDA UDI
878.4014 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Dry medical towel/wipe, single-use Skin cleaning wipe

Sage by Sage Products Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Sage Products Llc

Sources (1)

FDA UDI 4971ccf5-113e-4f57-a64e-15266f86ea4e 35 fields · synced Jun 8, 2026