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Prosphyg™ 768-609-11ABK

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 Number00634782094553 UDI-DI Date31 Aug 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  • Withdrawn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
Prosphyg™
Generic Name
Mechanical external stethoscope
Model / Ref / Catalog
768-609-11ABK
Primary DI / UDI-DI
00634782094553
FDA Product Code
LDE, DXQ
GMDN Term
Mechanical external stethoscope
Device Class
Class I
Regulation Number
870.1875, 870.1120
GUDID distribution status
In Commercial Distribution

Related devices

Category: Aneroid manual sphygmomanometerMechanical external stethoscope

Other devices from American Diagnostic Corporation

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Properties

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

Other properties (9)

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