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AincA® 00-380

by Anesthesia Associates, Inc.

AincA® 00-380 is a Class I device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B005003800), 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 NumberB005003800 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  • Withdrawn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
Mechanical external stethoscope
Model / Ref / Catalog
00-380
Description
Monoscope, Right-Ear, Size Small, w/ 42" Long Tubing x LuerF
Primary DI / UDI-DI
B005003800
FDA product code
BZS
GMDN term
Mechanical external stethoscope
Device class
Class I
Regulation number
868.1930
GUDID distribution status
In Commercial Distribution

Related devices

Category: Mechanical external stethoscope

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)