15 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATRIUM THORACIC CATHETER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ECHO SOUNDER EX-101EX 8 MHZ
FDA 510(k)
FDA Class 2
·Cardiovascular
CHEMTRUE(R) HCG PREGNANCY URINE MIDSTREAM TEST
FDA 510(k)
FDA Class 2
·Clinical Chemistry
RECEPTAL CANISTER 1000 ML CE
FDA Adverse Event
Malfunction
·AMSINO MEDICAL CO., LTD.·Product code GCX·May 25, 2012
RECEPTAL 1.5LITER PE/CE WITH (50/CASE)
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code GCX·August 1, 2011
NON-PVC RECEPT LINER 2000ML/CE(50/CS)
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code GCX·June 21, 2011
NON-PVC RECEPT. LINER 2000ML/CE(50/CS)
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code GCX·June 21, 2011
NON-PVC RECEPT LINER 2000ML/CE(50/CS)
FDA Adverse Event
Malfunction
·HOSPIRA, LTD.·Product code GCX·June 21, 2011
RECEPTAL 1.5 LITER PE/CE WITH (50/CASE)
FDA Adverse Event
Injury
·HOSPIRA LTD.·Product code GCX·November 18, 2010
RECEPTAL 1 LITER/CE WITH VALVE (50/CAS)
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code GCX·June 24, 2011
RECEPTAL 1 LITER/CE WITH VALVE (50/CAS)
FDA Adverse Event
Malfunction
·HOSPIRA LTD.·Product code GCX·June 24, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC·Product code LKK·April 14, 2014
ANALYTICAL P MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·November 14, 2012
CSS CANNULATED SCREW SYSTEM
FDA Adverse Event
Injury
·ORTHOHELIX SURGICAL DESIGN·Product code HWC·September 7, 2010
BARD Dynamic XT Deca Steerable, Product Number 201102, REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026