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Scavenger, Eavs, Midas Eavs-5000

by Parker Hannifin Corp.

Scavenger, Eavs, Midas Eavs-5000 is a Class II device made by Parker Hannifin Corp., cleared under FDA 510(k) K241465 on 19 Sep 2024 and listed in FDA GUDID since 21 Feb 2025 (UDI-DI 00816711024224), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K241465

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816711024224 UDI-DI Date21 Feb 2025ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK241465 Date19 Sep 2024DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K241465 decided 19 Sep 2024 Active
  • FDA GUDID UDI-DI 00816711024224 listed 21 Feb 2025 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K241465
  2. Listed FDA GUDID 00816711024224

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Scavenger, Eavs, Midas
Generic name
Anaesthesia workstation gas scavenger
Model / Ref / Catalog
EAVS-5000
Primary DI / UDI-DI
00816711024224
510(k) Number
FDA product code
CBN
GMDN term
Anaesthesia workstation gas scavenger
Device class
Class II
Regulation number
868.5430
GUDID distribution status
In Commercial Distribution

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Properties

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