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DeVilbiss DV53BR

by DeVilbiss Healthcare LLC.

DeVilbiss DV53BR is a Class II device made by DeVilbiss Healthcare LLC., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00885304000389), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00885304000389 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Home CPAP unit
Model / Ref / Catalog
DV53BR
Primary DI / UDI-DI
00885304000389
FDA product code
BZD
GMDN term
Home CPAP unit
Device class
Class II
Regulation number
868.5905
GUDID distribution status
Not in Commercial Distribution

Other devices from DeVilbiss Healthcare LLC.

See all devices from DeVilbiss Healthcare LLC. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)