← Back to catalogue

Coe®

FDA UDI

Class I (US FDA UDI)

by Gc America Inc.

Identity

Trade Name
COE® FDA UDI
Generic Name
Medical device-decontamination agent FDA UDI
Device Name
COEfect™ MinuteWipe Qty. 100 Pre-treated Wipes (7" x 9") FDA UDI
Model / Reference
557200 FDA UDI
Description
COEfect™ MinuteWipe Qty. 100 Pre-treated Wipes (7" x 9") FDA UDI

Identifiers

Catalog Number
557200 FDA UDI
Primary DI / UDI-DI
D6585572001 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Medical device-decontamination agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 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

Yes

FDA UDI

Over-the-Counter

No

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: Medical device-decontamination agent

Coe® by Gc America Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device-decontamination agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Gc America Inc.

Sources (1)

  • FDA UDI a5606646-efb1-4b54-8576-67771e0103cc 35 fields · synced Jun 8, 2026