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Evolyse

FDA UDI

Class I (US FDA UDI)

by Amil Care Corporation

Identity

Trade Name
Evolyse FDA UDI
Generic Name
Medical device disinfection agent FDA UDI
Device Name
Aerial disinfectant for non-invasive medical devices and surfaces FDA UDI
Model / Reference
basic 2L FDA UDI
Description
Aerial disinfectant for non-invasive medical devices and surfaces FDA UDI

Identifiers

Catalog Number
2020.21 FDA UDI
Primary DI / UDI-DI
G0602020210 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Medical device disinfection 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Category: Medical device disinfection agent

Evolyse by Amil Care Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device disinfection agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ef7616ba-1d7c-49a3-94bd-b22354983c12 34 fields · synced Jun 7, 2026