co_sos
1 records
fda
7 records
FDA Device Recall: AirTouch F20 Full Face Mask and User Guide
2023-12-27
Class I — Masks non-invasive interface for channeling airflow to patients have magnets that have potential magnetic interference with active medical implants that interact with magnets, and metallic i...
View Source
FDA Device Recall: AirTouch N20 Nasal Mask and User Guide
2023-12-27
Class I — Masks non-invasive interface for channeling airflow to patients have magnets that have potential magnetic interference with active medical implants that interact with magnets, and metallic i...
View Source
FDA Device Recall: AirFit F30 Full Face Mask and User Guide
2023-12-27
Class I — Masks non-invasive interface for channeling airflow to patients have magnets that have potential magnetic interference with active medical implants that interact with magnets, and metallic i...
View Source
FDA Device Recall: AirFit N10 Nasal Masks and User Guide
2023-12-27
Class I — Masks non-invasive interface for channeling airflow to patients have magnets that have potential magnetic interference with active medical implants that interact with magnets, and metallic i...
View Source
FDA Device Recall: Astral 100 and Astral 150 ventilators
2023-11-01
Class I — If ventilator is on internal battery, not intended to serve as a primary power source, low/critically low battery alarms will sound, but a fault leads to sudden power loss. If power fails, t...
View Source
FDA Device Recall: Quattro Air FFM MED AMER, Product Code: 62702, full face mask for use with ac
2016-08-24
Class II — Masks in this lot, labelled and sold as 62702 vented Quattro Air FFM size Medium actually contain a non-vented (NV) Quattro Air FFM Large mask.
View Source
FDA Device Recall: Astral 100, 150 Model: 27001, 27003 In the US, Astral devices are primarily us
2016-02-10
Class II — Resmed Corporation is recalling Astral 100, 150 External Battery because of a start-up issue.
View Source
lobbying
3 records
Lobbying Client: RESMED CORP.
Lobbied by DLA PIPER LLP (US) — Medical device manufacturer and digital health company.
View Source
Lobbying Client: RESMED CORP.
Lobbied by DLA PIPER LLP (US) — Medical device manufacturer and digital health company.
View Source
Lobbying Client: RESMED CORP.
Lobbied by ICE MILLER LLP — Manufacturer of cloud-connected medical devices for people with sleep apnea, COPD, etc.
View Source
ny_corps
1 records
NY Corp: RESMED CORP.
1994-05-13
FOREIGN BUSINESS CORPORATION | County: Monroe | Jurisdiction: Minnesota
View Source
SEC EDGAR
1 records
Be informed when major changes happen on C.F.A.I. — new data sources, platform updates, critical enforcement alerts
No spam. Only major updates. Unsubscribe anytime.