Aicon JJ725

by Aesculap, Inc.

Aicon JJ725 is a Class II device made by Aesculap, Inc., listed in FDA GUDID since 25 Feb 2022 (UDI-DI 04046955292349), registry data as of 22 Oct 2026.

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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04046955292349 UDI-DI	Date25 Feb 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04046955292349

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Aicon
Generic name: Chemical/physical sterilization process indicator
Model / Ref / Catalog: JJ725

Primary DI / UDI-DI: 04046955292349
FDA product code: KCT
GMDN term: Chemical/physical sterilization process indicator

Device class: Class II
Regulation number: 880.6850
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Properties

Sterilise before use
Single use
Over-the-counter
Lot / batch number
Expiration date

Other properties (10, all answered No)