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Diagnostix™ 5681L-346L7EUW

by American Diagnostic Corporation

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

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 Number00634782092399 UDI-DI Date9 Feb 2018ListedStatusListed 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  • Withdrawn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
Diagnostix™
Generic Name
Aneroid manual sphygmomanometer
Model / Ref / Catalog
5681L-346L7EUW
Primary DI / UDI-DI
00634782092399
FDA Product Code
DXQ, FLL, ERA, HLJ
GMDN Term
Aneroid manual sphygmomanometer
Device Class
Class II
Regulation Number
870.1120, 880.2910, 874.4770, 886.1570
GUDID distribution status
In Commercial Distribution

Related devices

Category: Aneroid manual sphygmomanometerOphthalmic/otologic diagnostic setInfrared patient thermometer, skin

Other devices from American Diagnostic Corporation

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Properties

  • Over-the-Counter
  • Convenience Kit
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No