45 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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C.T.M. MOBILITY SCOOTERS HS-666, HS-730, HS-570
FDA 510(k)
FDA Class 2
·Physical Medicine
PowerPICC SOLO
FDA UDI
Bard Access Systems, Inc.·00801741087431·Catheter Placement Kit
ASIA MED
FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282500221·asia-med Special No. 19: coated acupuncture ne...
ASIA MED
FDA UDI
asia-med GmbH·04251282507541·asia-med Special No. 19: coated acupuncture ne...
Bard Button Device Decompression Tube
FDA UDI
Bard Access Systems, Inc.·00801741080982·24 Fr. x 2.4 Button Decompression Tube
Zavation
FDA UDI
Zavation LLC·00842166122079·3-Level, 54mm Cervical Plate
RETAINER KIT
FDA UDI
Access Dental Lab, LLC·00850007728038·RETAINER KIT
Mariner MIS
FDA UDI
Seaspine Orthopedics Corporation·10889981182281·EXTENDED TAB BODY CT
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700003540·
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700003540·
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·June 24, 2024
FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN
FDA 510(k)
FDA Unclassified
·Unknown
ELIACHAR LARYNGEAL FOAM STENT, MODEL ELL-1
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·February 27, 2025
SURGISTOOL
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FZM·March 12, 2013
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·February 18, 2011
BIOPINCE
FDA Adverse Event
Malfunction
·MEDICAL DEVICE TECHNOLOGIES INC.·Product code KNW·January 18, 2008
HUDSON NEBULIZER ADAPTOR 033, STERILE, JAPANESE
FDA Adverse Event
Malfunction
·TELEFLEX·Product code CCQ·September 15, 2014
HUDSON NEBULIZER ADAPTER 033, STERILE, JAPANESE
FDA Adverse Event
Malfunction
·TELEFLEX·Product code CCQ·October 23, 2014
HUDSON NEBULIZER ADAPTOR 033, STERILE, JAPANESE
FDA Adverse Event
Malfunction
·TELEFLEX·Product code CCQ·October 23, 2014