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AincA 00-250

by Anesthesia Associates, Inc.

AincA 00-250 is a Class II device made by Anesthesia Associates, Inc., listed in FDA GUDID since 19 Aug 2016 (UDI-DI B005002500), 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 NumberB005002500 UDI-DI Date19 Aug 2016ListedStatusListed 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  • Withdrawn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
Mechanical expiratory valve, reusable
Model / Ref / Catalog
00-250
Primary DI / UDI-DI
B005002500
FDA product code
BYE
GMDN term
Mechanical expiratory valve, reusable
Device class
Class II
Regulation number
868.5965
GUDID distribution status
In Commercial Distribution

Related devices

Category: Mechanical expiratory valve, reusable

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)