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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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83 records meeting your search criteria returned- Product Code: CAI Patient Problem: No Patient Involvement Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
NULL PORTEX 03/04/2021
NULL PORTEX 01/18/2021
NULL PORTEX 01/18/2021
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX 01/10/2021
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX 01/05/2021
NULL PORTEX 01/02/2021
NULL PORTEX 01/02/2021
NULL PORTEX GENERAL ANESTHESIA CIRCUITS 12/31/2020
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX GENERAL ANESTHESIA CIRCUITS 12/17/2020
NULL PORTEX 12/13/2020
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