Skip to content

Aesculap US906

by Aesculap, Inc.

Aesculap US906 is a Class II device made by Aesculap, Inc., listed in FDA GUDID since 22 Sep 2016 (UDI-DI 05055049007423), 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

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05055049007423 UDI-DI Date22 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Aesculap
Generic name
Chemical/physical sterilization process indicator
Model / Ref / Catalog
US906
Primary DI / UDI-DI
05055049007423
FDA product code
JOJ
GMDN term
Chemical/physical sterilization process indicator
Device class
Class II
Regulation number
880.2800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Chemical/physical sterilization process indicator

Similar devices in this category

Other devices filed under Chemical/physical sterilization process indicator.

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)