10 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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True Dilatation Balloon Valvuloplasty Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
TruLink
FDA UDI
OSI OPTOELECTRONICS, INC.·00859998006453·SpO2 Cloth Sensor Single-patient Use - Neonate
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171028345·PESSARY, GEHRUNG #6, 80mm
Trulink
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522102387·SENSOR,SPO2,CLOTH,NEO,SPU,24/BX,ROHS
R2 FAMILY OF IMAGE DISPLAY UNITS WITH R2 UNIFORM DISPLAY SOFTWARE
FDA 510(k)
FDA Class 2
·Radiology
IMAGE-ARENA AND IMAGE-ARENA APPLICATIONS
FDA 510(k)
FDA Class 2
·Radiology
A7 ANESTHESIA SYSTEM
FDA Adverse Event
Malfunction
·SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO. LTD.·Product code BSZ·February 15, 2017
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014
PK DISSECTING FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·June 6, 2013
PFNA BLADE
FDA Adverse Event
Injury
·SYNTHES BETTLACH·Product code KTT·June 24, 2011