Enzol™ 2252

by Advanced Sterilization Products Services Inc.

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number10705037018062 UDI-DI	Date16 Dec 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Enzol™
Generic Name: Medical device cleaning agent
Model / Ref / Catalog: 2252

Primary DI / UDI-DI: 10705037018062
FDA Product Code: FLG
GMDN Term: Medical device cleaning agent

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

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See all devices from Advanced Sterilization Products, Inc. →

Properties

Over-the-Counter
Premarket Exempt
Lot / Batch Number
Expiration Date

Other properties (10)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Serial Number: No
Manufacturing Date: No