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ViaMed 13410-MIX

by Rece International Corp.

ViaMed 13410-MIX is a Class I device made by Rece International Corp., listed in FDA GUDID since 27 Nov 2020 (UDI-DI 00811382011467), 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 Number00811382011467 UDI-DI Date27 Nov 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  • Withdrawn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
ViaMed
Generic name
Mechanical external stethoscope
Model / reference
13410-MIX
Primary DI / UDI-DI
00811382011467
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 Rece International Corp.

  • ViaMed 17318-R

    Class II

  • ViaMed 13450-BLACK

    Class II

  • ViaMed 13312-BLUE

    Class II

  • ViaMed 17001-R

    Class II

See all devices from Rece International Corp. →

Properties

  • Contains latex
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)