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Vpap 26923

by Resmed Pty Ltd

Vpap 26923 is a Class II device made by Resmed Pty Ltd, listed in FDA GUDID since 13 Sep 2016 (UDI-DI 00619498269235), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00619498269235 UDI-DI Date13 Sep 2016ListedStatusListed 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  • Withdrawn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
Vpap
Generic name
Home BPAP unit
Model / Ref / Catalog
26923
Primary DI / UDI-DI
00619498269235
FDA product code
MNS
GMDN term
Home BPAP unit
Device class
Class II
Regulation number
868.5895
GUDID distribution status
In Commercial Distribution

Related devices

Category: Home BPAP unit

Similar devices

Other devices filed under FDA product code MNS (Ventilator, Continuous, Non-Life-Supporting).

Other devices from Resmed Pty Ltd

See all devices from Resmed Pty Ltd →

Properties

  • Lot / batch number
Other properties (14, all answered No)