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Ventilator Filter VF005-2

by SUNSET HEALTHCARE SOLUTIONS, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00848530108939 UDI-DI Date30 Apr 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Ventilator Filter
Generic Name
Local/regional anaesthesia conduction filter
Model / Reference
VF005-2
Description
Sunset Particulate Filter for Respironics Trilogy Ventilator – 2/PK
Primary DI / UDI-DI
00848530108939
FDA Product Code
JRL
GMDN Term
Local/regional anaesthesia conduction filter
Device Class
Class I
Regulation Number
862.2050
GUDID distribution status
In Commercial Distribution

Other devices from SUNSET HEALTHCARE SOLUTIONS, Inc.

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Properties

  • Single Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No