13 results
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27ms
·
Sources: EU EUDAMED, US FDA
Timberline® Lateral Interbody Fusion System
FDA UDI
BIOMET SPINE LLC·00887868203008·
Timberline® Lateral Interbody Fusion System
FDA UDI
BIOMET SPINE LLC·00887868201745·
Timberline Lateral Fusion System
FDA UDI
Highridge Medical, LLC·03662663258630·Spacer Lat PEEK 0° CT 55L X 26W X 50H
TIMBERLINE LATERAL FUSION SYSTEM
FDA UDI
BIOMET SPINE LLC·00888480563518·
TIMBERLINE LATERAL FUSION SYSTEM
FDA UDI
BIOMET SPINE LLC·00888480562863·
TIMBERLINE LATERAL FUSION SYSTEM
FDA UDI
BIOMET SPINE LLC·00888480564126·
Timberline Lateral Fusion System
FDA UDI
Highridge Medical, LLC·03662663257374·Spacer Lat PEEK 0° 55L X 26W X 50H
Timberline® Lateral Interbody Fusion System
FDA UDI
BIOMET SPINE LLC·00887868202391·
Timberline Lateral Fusion System
FDA UDI
Highridge Medical, LLC·03662663258029·Spacer Lat PEEK 8° 55L X 26W X 50H
SUCTION APPARATUS, PATIENT CARE
FDA Adverse Event
EMG TECHNOLOGY CO. LTD·Product code DWM·May 24, 2013
FLOTATION CUSHION
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code KIC·January 7, 2013
STYLE 68 SALINE FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·June 17, 2019
FLOTATION CUSHION
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code KIC·October 12, 2011