9 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACKRAD ESOPHAGEAL BALLOON CATHETER SET
FDA 510(k)
FDA Class 2
·Anesthesiology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704920928·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704284614·BECKMAN-WEITLANER RETRACTOR 9 1/2" 3X4 SHARP
DILATING TIP TROCAR WITH STABILITY SLEEVE - 12MM DIAMETER
FDA Adverse Event
Injury
·Product code GCJ·June 20, 2006
Powder Free Nitrile Examination Glove (Blue) With Low Dermatitis Potential Claim and with tested for Use with Chemotherapy Drugs
FDA 510(k)
FDA Class 1
·General Hospital
ACCOLADE RPS HIP STEM
FDA 510(k)
FDA Class 2
·Orthopedic
TANDEM T: SLIM INSULIN DELIVERY SYS
FDA Adverse Event
Malfunction
·TANDEM DIABETES·Product code LZG·May 15, 2014
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·February 9, 2013
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 7, 2011