11 results
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17ms
·
Sources: EU EUDAMED, US FDA
ANSWER OVULATION TEST KIT
FDA 510(k)
FDA Class 1
·Clinical Chemistry
NA
FDA UDI
KEY SURGICAL, INC.·10849771049453·K-Wires, Single diamond, round end, .035-inch (...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293135·
Key Surgical K-Wires and Steinmann Pins
FDA UDI
KEY SURGICAL, INC.·00849771012832·K-Wires, Single diamond, round end, .035-inch (...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659484603·K-Wire w. lanzet/round end _x000D_...
K-Wire w. lanzet/round end 0.89mm/229mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM712410·K-Wire w. lanzet/round end
0.89mm...
Pulse Oximeter
FDA 510(k)
FDA Class 2
·Cardiovascular
LMS-LIVER
FDA 510(k)
FDA Class 2
·Radiology
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC., SLEEP & HOME RESPIRATORY GROUP·Product code CBK·April 16, 2014
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 15, 2010
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 12, 2012