AincA® 00-414

by Anesthesia Associates, Inc.

AincA® 00-414 is a Class I device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B005004140), 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	NumberB005004140 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Withdrawn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: Low-pressure tubing connector, reusable
Model / Ref / Catalog: 00-414

Primary DI / UDI-DI: B005004140
FDA product code: BZA
GMDN term: Low-pressure tubing connector, reusable

Device class: Class I
Regulation number: 868.5810
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)