AincA® 00-184

by Anesthesia Associates, Inc.

AincA® 00-184 is a Class I device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B005001840), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB005001840 UDI-DI	Date31 Mar 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: AincA®
Generic name: Straight/elbow breathing circuit connector, reusable
Model / Ref / Catalog: 00-184

Primary DI / UDI-DI: B005001840
FDA product code: CAI
GMDN term: Straight/elbow breathing circuit connector, reusable

Device class: Class I
Regulation number: 868.5240
GUDID distribution status: In Commercial Distribution

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See all devices from Anesthesia Associates, Inc. →

Properties

Prescription use
Premarket exempt
Lot / batch number

Other properties (12, all answered No)