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ResScan 31335

by Resmed Pty Ltd

ResScan 31335 is a Class II device made by Resmed Pty Ltd, listed in FDA GUDID since 8 Nov 2019 (UDI-DI 00619498313358), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00619498313358 UDI-DI Date8 Nov 2019ListedStatusListed 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  • Withdrawn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 / Ref / Catalog
31335
Primary DI / UDI-DI
00619498313358
FDA product code
MNS, MNT, BZD, CBK
GMDN term
Ventilator application software
Device class
Class II
Regulation number
868.5895, 868.5905
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ventilator application software

Similar devices

Other devices filed under FDA product code MNS (Ventilator, Continuous, Non-Life-Supporting).

Other devices from Resmed Pty Ltd

See all devices from Resmed Pty Ltd →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)