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A&D Medical UA-606

by A & D Co., Ltd.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00093764604744 UDI-DI Date25 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
A&D Medical
Generic Name
Automatic-inflation electronic sphygmomanometer, non-portable
Model / Ref / Catalog
UA-606
Primary DI / UDI-DI
00093764604744
510(k) Number
FDA Product Code
DXN
GMDN Term
Automatic-inflation electronic sphygmomanometer, non-portable
Device Class
Class II
Regulation Number
870.1130
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K141160)

Other devices from A & D Co., Ltd.

See all devices from A & D Co., Ltd. →

Properties

  • Over-the-Counter
  • Serial Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No