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SimplyGo Mini, INTL

by Respironics Inc.

SimplyGo Mini, INTL (1113603) is a Class II device made by Respironics Inc., listed in FDA GUDID since 16 Jan 2017 (UDI-DI 00606959032415), 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 Number00606959032415 UDI-DI Date16 Jan 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  • Withdrawn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
SimplyGo Mini
Generic name
Mobile/portable oxygen concentrator
Model / Ref / Catalog
SimplyGo Mini, INTL, 1113603
Primary DI / UDI-DI
00606959032415
FDA product code
CAW
GMDN term
Mobile/portable oxygen concentrator
Device class
Class II
Regulation number
868.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Mobile/portable oxygen concentrator

Similar devices in this category

Other devices filed under Mobile/portable oxygen concentrator.

Other devices from Respironics Inc.

See all devices from Respironics Inc. →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)