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3M™ Sps-YA1100

by 3M Company

3M™ Sps-YA1100 is a Class I device made by 3M Company, listed in FDA GUDID since 24 Sep 2018 (UDI-DI 00707387784201), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00707387784201 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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
3M™
Generic name
Mechanical external stethoscope
Model / Ref / Catalog
SPS-YA1100
Primary DI / UDI-DI
00707387784201
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

Other devices from 3M Company

See all devices from 3M Company →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)