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Sklar® 06-1654

by Sklar Corporation

Sklar® 06-1654 is a Class I device made by Sklar Corporation, listed in FDA GUDID since 7 Feb 2018 (UDI-DI 10649111348655), 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 Number10649111348655 UDI-DI Date7 Feb 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  • Withdrawn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
Sklar®
Generic name
Mechanical external stethoscope
Model / reference
06-1654
Primary DI / UDI-DI
10649111348655
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 Sklar Corporation

See all devices from Sklar Corporation →

Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (12, all answered No)