9 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MICRONAIL Distal Radius System
FDA 510(k)
FDA Class 2
·Orthopedic
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100011·BARRAQUER WIRE SPECULUM LARGE WITH TABS
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100202·NEVYAS DRAPE SPECULUM OPEN WIRE
Vertical Alignment Rod
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215056940·
INFX-8000V WITH
FDA 510(k)
FDA Class 2
·Radiology
MODIFICATION TO AMPHIRION DEEP 0.014 OTW PTA BALLOON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 7, 2014
PROPAQ MD DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·May 21, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 5, 2011