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S9 36377

by Resmed Pty Ltd

S9 36377 is a Class II device made by Resmed Pty Ltd, listed in FDA GUDID since 12 Jul 2019 (UDI-DI 00619498363773), 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 Number00619498363773 UDI-DI Date12 Jul 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  • Withdrawn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
S9
Generic name
Home BPAP unit
Model / Ref / Catalog
36377
Primary DI / UDI-DI
00619498363773
FDA product code
BZD
GMDN term
Home BPAP unit
Device class
Class II
Regulation number
868.5905
GUDID distribution status
In Commercial Distribution

Related devices

Category: Home BPAP unit

Similar devices

Other devices filed under FDA product code BZD (Ventilator, Non-Continuous (Respirator)).

Other devices from Resmed Pty Ltd

See all devices from Resmed Pty Ltd →

Properties

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