Skip to content

AincA® 00-417

by Anesthesia Associates, Inc.

AincA® 00-417 is a Class I device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B005004170), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB005004170 UDI-DI Date31 Mar 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
AincA®
Generic name
Breathing circuit tube holder
Model / Ref / Catalog
00-417
Primary DI / UDI-DI
B005004170
FDA product code
JAY
GMDN term
Breathing circuit tube holder
Device class
Class I
Regulation number
868.5280
GUDID distribution status
In Commercial Distribution

Related devices

Category: Breathing circuit tube holder

Similar devices

Other devices filed under FDA product code JAY (SUPPORT, BREATHING TUBE).

Other devices from Anesthesia Associates, Inc.

See all devices from Anesthesia Associates, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)