Prolystica 1C2308

by Steris Corporation

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00724995154363 UDI-DI	Date5 May 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Prolystica
Generic Name: Medical device cleaning agent
Model / Ref / Catalog: 1C2308

Primary DI / UDI-DI: 00724995154363
FDA Product Code: FLG
GMDN Term: Medical device cleaning agent

Device Class: Class I
Regulation Number: 880.6150
GUDID distribution status: In Commercial Distribution

Other devices from Steris Corporation

Alyon

Class I
Amsco

Class IIa
Prolystica

Class I
Revital-Ox

Class I
AMSCO 300 Accessory

Class I
Steris

Class I

See all devices from Steris Corporation →

Properties

Prescription Use
Premarket Exempt
Lot / Batch Number
Expiration Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Manufacturing Date: No