Skip to content

iCodeConnect Software 420002

by Bmc Medical., Ltd.

iCodeConnect Software 420002 is a Class II device made by Bmc Medical., Ltd., listed in FDA GUDID since 16 Jun 2017 (UDI-DI 06948538362075), 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 Number06948538362075 UDI-DI Date16 Jun 2017ListedStatusListed 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  • Withdrawn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
iCodeConnect Software
Generic name
Ventilator application software
Model / reference
420002
Primary DI / UDI-DI
06948538362075
FDA product code
BZD
GMDN term
Ventilator application software
Device class
Class II
Regulation number
868.5905
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code BZD (Ventilator, Non-Continuous (Respirator)).

Other devices from Bmc Medical., Ltd.

See all devices from Bmc Medical., Ltd. →

Properties

  • Prescription use
Other properties (14, all answered No)