Scavenger, Eavs, Midas Eavs-5000
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
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00816711024224 | Date21 Feb 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK241465 | Date19 Sep 2024 | StatusActive |
Official records
- AccessGUDID record 00816711024224
- FDA 510(k) database K241465
Across registries
- FDA 510(k) K241465 decided 19 Sep 2024 Active
- FDA GUDID UDI-DI 00816711024224 listed 21 Feb 2025 Listed
Timeline
- Cleared FDA 510(k) K241465
- Listed FDA GUDID 00816711024224
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 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
Similar devices in this category
Other devices filed under Anaesthesia workstation gas scavenger.