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DeVilbiss 555DS-R

by DeVilbiss Healthcare LLC.

DeVilbiss 555DS-R is a Class II device made by DeVilbiss Healthcare LLC., listed in FDA GUDID since 20 Aug 2026 (UDI-DI 00885304035817), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885304035817 UDI-DI Date20 Aug 2026ListedStatusListed 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  • Withdrawn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
DeVilbiss
Generic name
Stationary oxygen concentrator
Model / Ref / Catalog
555DS-R
Primary DI / UDI-DI
00885304035817
FDA product code
CAW
GMDN term
Stationary oxygen concentrator
Device class
Class II
Regulation number
868.5440
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Size
Height — 18.4 Inch
Width — 14.6 Inch
Length — 9.9 Inch

Other devices from DeVilbiss Healthcare LLC.

See all devices from DeVilbiss Healthcare LLC. →

Properties

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