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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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4 records meeting your search criteria returned- Product Code: CAC Product Problem: Unsealed Device Packaging Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
TELEFLEX MEDICAL PE PNEUMONECTOMY LF 6/CS 09/13/2021
TELEFLEX MEDICAL PE SAHARA DRY SUCT/DRY SEAL LF 6/CS 08/31/2017
TELEFLEX MEDICAL PE SAHARA DRY SUCT/DRY SEAL LF 6/CS 08/31/2017
TELEFLEX MEDICAL PE SAHARA DRY SUCT/DRY SEAL LF 6/CS 08/31/2017
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