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Aesculap US994

by Aesculap, Inc.

Aesculap US994 is a Class II device made by Aesculap, Inc., listed in FDA GUDID since 22 Sep 2016 (UDI-DI 04046964930812), 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 Number04046964930812 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  • Withdrawn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
Sterilization container filter, single-use
Model / Ref / Catalog
US994
Primary DI / UDI-DI
04046964930812
FDA product code
KCT, FRG
GMDN term
Sterilization container filter, single-use
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Sterilization container filter, single-use

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)