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AincA® LF-719-20

by Anesthesia Associates, Inc.

AincA® LF-719-20 is a Class I device made by Anesthesia Associates, Inc., listed in FDA GUDID since 17 Aug 2023 (UDI-DI B005LF719200), 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 NumberB005LF719200 UDI-DI Date17 Aug 2023ListedStatusListed 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  • Withdrawn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 bag, reusable
Model / Ref / Catalog
LF-719-20
Primary DI / UDI-DI
B005LF719200
FDA product code
BTC
GMDN term
Breathing circuit bag, reusable
Device class
Class I
Regulation number
868.5320
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Total Volume — 2.0 Liter

Related devices

Category: Breathing circuit bag, reusable

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Other devices filed under Breathing circuit bag, reusable.

Other devices from Anesthesia Associates, Inc.

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Properties

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