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Stethoscope 121-PUR

by Rashman Corp.

Stethoscope 121-PUR is a Class I device made by Rashman Corp., listed in FDA GUDID since 2 Dec 2022 (UDI-DI 00786511788599), 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 Number00786511788599 UDI-DI Date2 Dec 2022ListedStatusListed 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  • Withdrawn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
Stethoscope
Generic name
Mechanical external stethoscope
Model / reference
121-PUR
Primary DI / UDI-DI
00786511788599
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 in this category

Other devices filed under Mechanical external stethoscope.

Other devices from Rashman Corp.

See all devices from Rashman Corp. →

Properties

  • Premarket exempt
Other properties (14, all answered No)