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Omron Sprague Rappaport Stethoscope 416-22-DB

by Omron Healthcare, Inc.

Listed FDA GUDID listing, not in commercial distribution

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 Number00073796416027 UDI-DI Date13 Jul 2020ListedStatusListed GUDID: not 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  • Withdrawn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
Omron Sprague Rappaport Stethoscope
Generic Name
Mechanical external stethoscope
Model / Ref / Catalog
416-22-DB
Primary DI / UDI-DI
00073796416027
FDA Product Code
LDE
GMDN Term
Mechanical external stethoscope
Device Class
Class I
Regulation Number
870.1875
GUDID distribution status
Not in Commercial Distribution

Other devices from Omron Healthcare, Inc.

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Properties

  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

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