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Prolystica

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
Prolystica FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
Prolystica HP Alkaline Automated Detergent 2.5-Gallon is formulated specifically for automated washing with a low foam profile, corrosion inhibitors for superior instrument and equipment protection, and broad-spectrum substrate compatibility. FDA UDI
Model / Reference
1C2010 FDA UDI
Description
Prolystica HP Alkaline Automated Detergent 2.5-Gallon is formulated specifically for automated washing with a low foam profile, corrosion inhibitors for superior instrument and equipment protection, and broad-spectrum substrate compatibility. FDA UDI

Identifiers

Catalog Number
1C2010 FDA UDI
Primary DI / UDI-DI
00724995154455 FDA UDI
FDA Product Code
FLG FDA UDI
GMDN Term
Medical device cleaning agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6150 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

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: Medical device cleaning agent

Prolystica by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 1f5f75b3-1c76-4702-bc3f-e35de49ed922 35 fields · synced Jun 8, 2026