23 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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REDSENSE ALARM SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450116913·
LINK Instruments - Rasps, compressors and broaches
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575426416·Orthopaedic broach - SPII Model Lubinus Hip Stem
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197047609·Brown Tissue Forceps
7x7 te...
LINK Instruments - Rasps, compressors and broaches
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575426454·Orthopaedic broach - SPII Model Lubinus Hip Stem
LINK Instruments - Rasps, compressors and broaches
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575426423·Orthopaedic broach - SPII Model Lubinus Hip Stem
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197527491·Brown surgical forceps 7x7 teeth, 250mm
250mm
LINK Instruments - Rasps, compressors and broaches
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575426430·Orthopaedic broach - SPII Model Lubinus Hip Stem
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197047623·Brown Tissue Forceps
7x7 te...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197509695·Cushing-Brown Tissue Forceps
9x9 te...
LINK Instruments - Rasps, compressors and broaches
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575426409·Orthopaedic broach - SPII Model Lubinus Hip Stem
LINK Instruments - Rasps, compressors and broaches
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575426447·Orthopaedic broach - SPII Model Lubinus Hip Stem
LINK Instruments - Rasps, compressors and broaches
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575426393·Orthopaedic broach - SPII Model Lubinus Hip Stem
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197047593·Adson Fixation Forceps
straig...
RESPIRATORY HUMIDIFIER , HEATED DELIVERY SYSTEM, ADAPTOR, MODELS MR880, RT241, 900MR441
FDA 510(k)
FDA Class 2
·Anesthesiology
CALLOS
FDA 510(k)
FDA Class 2
·Orthopedic
RESTORE ADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·February 27, 2013
LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·September 25, 2018
PROFEMUR(R) MODULAR FEMORAL NECK
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·May 24, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·September 30, 2014