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DreamStation 00

by Respironics Inc. 16 variants

DreamStation 00 (200675C) is a Class I device made by Respironics Inc., listed in FDA GUDID since 29 Dec 2019 (UDI-DI 00606959058224), 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 Number00606959058224 UDI-DI Date29 Dec 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  • Withdrawn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
DreamStation
Generic name
Clinical laboratory information system
Model / Ref / Catalog
00, 200675C
Primary DI / UDI-DI
00606959058224
FDA product code
OUG
GMDN term
Clinical laboratory information system
Device class
Class I
Regulation number
880.6310
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code OUG (Medical device data system).

Other devices from Respironics Inc.

See all devices from Respironics Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)