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SmartVest I-VCS-24

by Electromed, Inc.

SmartVest I-VCS-24 is a Class II device made by Electromed, Inc., listed in FDA GUDID since 30 Jun 2016 (UDI-DI B102060171S0100), 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 NumberB102060171S0100 UDI-DI Date30 Jun 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
SmartVest
Generic name
Chest-oscillation airway secretion-clearing system vest
Model / Ref / Catalog
I-VCS-24
Description
SPU SmartVest® – Child Small
Primary DI / UDI-DI
B102060171S0100
FDA product code
BYI
GMDN term
Chest-oscillation airway secretion-clearing system vest
Device class
Class II
Regulation number
868.5665
GUDID distribution status
In Commercial Distribution

Related devices

Category: Chest-oscillation airway secretion-clearing system vest

Similar devices

Other devices filed under FDA product code BYI (Percussor, Powered-Electric).

Other devices from Electromed, Inc.

See all devices from Electromed, Inc. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)