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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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11 records meeting your search criteria returned- Product Code: BTR Product Problem: Unsealed Device Packaging Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX TUBES BLUE LINE CLASSIC 08/25/2023
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX ENDOTRACHEAL TUBES POLAR 04/17/2023
SMITHS MEDICAL INTERNATIONAL, LTD. INTUBATION- PORTEX ENDOTRACHEAL TUBE 09/07/2022
SMITHS MEDICAL ASD, INC. FOME-CUF-WIRE RE-ENFORCED, AIRE-CUF WIRE 09/04/2022
SMITHS MEDICAL ASD, INC. FOME-CUF-WIRE RE-ENFORCED, AIRE-CUF WIRE 09/04/2022
SMITHS MEDICAL ASD, INC. FOME-CUF-WIRE RE-ENFORCED, AIRE-CUF WIRE 09/04/2022
SMITHS MEDICAL ASD, INC. FOME-CUF-WIRE RE-ENFORCED, AIRE-CUF WIRE 09/04/2022
SMITHS MEDICAL ASD, INC. FOME-CUF-WIRE RE-ENFORCED, AIRE-CUF WIRE 09/04/2022
SMITHS MEDICAL ASD, INC. FOME-CUF-WIRE RE-ENFORCED, AIRE-CUF WIRE 09/03/2022
SMITHS MEDICAL INTERNATIONAL, LTD. PORTEX SILICONISED PVC, ORAL/NASAL 06/24/2022
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