Skip to content

RMDpulse 22253

by Resmed Corp

RMDpulse 22253 is a Class II device made by Resmed Corp, listed in FDA GUDID since 13 Apr 2021 (UDI-DI 00840193400030), 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 Number00840193400030 UDI-DI Date13 Apr 2021ListedStatusListed 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  • Withdrawn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
RMDpulse
Generic name
Ventilator application software
Model / reference
22253
Primary DI / UDI-DI
00840193400030
FDA product code
BZD
GMDN term
Ventilator application software
Device class
Class II
Regulation number
868.5905
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ventilator application software

Similar devices

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

Other devices from Resmed Corp

See all devices from Resmed Corp →

Properties

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