14 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SILVERLON ISLAND WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
ArgenZ HT+ 95x30 B4
FDA UDI
ARGEN CORPORATION, THE·D818122817·Dental porcelain/ceramic restoration kit
Zavation
FDA UDI
Zavation LLC·00842166188792·17mm Dilator
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
COOLTOUCH ND:YAG LASER SYSTEM, MODEL COOLTOUCH, COOLTOUCH-II ND:YAG LASER SYSTEM, MODEL COOLTOUCH-II
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CODA BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·October 23, 2017
UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·January 28, 2013
UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·January 28, 2013
UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·January 28, 2013
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 21, 2013
THE EMAX 2 PLUS SYSTEM
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·September 26, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 14, 2011
ACCESS® 2 IMMUNOASSAY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code MMI·February 5, 2013
CODA BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·September 10, 2019