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ResScan 31338

by Resmed Corp

ResScan 31338 is a Class II device made by Resmed Corp, listed in FDA GUDID since 24 Feb 2023 (UDI-DI 08401934313389), 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 Number08401934313389 UDI-DI Date24 Feb 2023ListedStatusListed 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  • Withdrawn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
ResScan
Generic name
Ventilator application software
Model / reference
31338
Primary DI / UDI-DI
08401934313389
FDA product code
BZD, CBK, MNS, MNT
GMDN term
Ventilator application software
Device class
Class II
Regulation number
868.5905, 868.5895
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
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)