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DeVilbiss DV5MB

by DeVilbiss Healthcare LLC.

DeVilbiss DV5MB is a Class II device made by DeVilbiss Healthcare LLC., listed in FDA GUDID since 8 Sep 2017 (UDI-DI 00885304008309), not in commercial distribution (GUDID) as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885304008309 UDI-DI Date8 Sep 2017ListedStatusListed 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  • Withdrawn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
DV5MB
Primary DI / UDI-DI
00885304008309
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)