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Astral 27915

by Resmed Pty Ltd

Astral 27915 is a Class I device made by Resmed Pty Ltd, listed in FDA GUDID since 30 Sep 2016 (UDI-DI 00619498279159), 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 Number00619498279159 UDI-DI Date30 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  • Withdrawn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
Astral
Generic name
Ventilator stand
Model / Ref / Catalog
27915
Primary DI / UDI-DI
00619498279159
FDA product code
BRY
GMDN term
Ventilator stand
Device class
Class I
Regulation number
868.6100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ventilator stand

Similar devices

Also classified as Ventilator stand.

Similar devices

Other devices filed under FDA product code BRY (Cabinet, Table And Tray, Anesthesia).

Other devices from Resmed Pty Ltd

See all devices from Resmed Pty Ltd →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)