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Greater Goods 0612

by Greater Goods, LLC

Greater Goods 0612 is a Class I device made by Greater Goods, LLC, listed in FDA GUDID since 31 Aug 2020 (UDI-DI 00875011006125), 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 Number00875011006125 UDI-DI Date31 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Greater Goods
Generic name
Mechanical external stethoscope
Model / reference
0612
Primary DI / UDI-DI
00875011006125
FDA product code
LDE
GMDN term
Mechanical external stethoscope
Device class
Class I
Regulation number
870.1875
GUDID distribution status
In Commercial Distribution

Related devices

Category: Mechanical external stethoscope

Similar devices

Other devices filed under FDA product code LDE (Stethoscope, Manual).

Other devices from Greater Goods, LLC

See all devices from Greater Goods, LLC →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)