17 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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RAPID DRUG SCREEN 5-PANEL WITH METHAMPHETAMINE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ReLine
FDA UDI
Nuvasive, Inc.·00195377076823·RELINE C Screw, 4.5x25mm FA Thoracic M L
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984525·anteriors; shade C3; mould 90
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665587015·MIS Cannulated Screw M, Ø4.5 x 25mm, Ø6.0mm Rod
STILLE Forceps
FDA UDI
Stille AB·07332339202743·BJÖRK-STILLE FORCEPS insulated 25 cm 10 in
FPR PHENOBARBITAL KIT
FDA 510(k)
FDA Class 2
·Clinical Toxicology
PEDIATRIC HUMIDIFIER TUBE W/ TEMPERATURE PORT
FDA 510(k)
FDA Class 1
·Anesthesiology
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 27, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 27, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 18, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPAEDIC INC.·Product code KWP·October 8, 2009
TSRH SPINAL SYSTEM
FDA Adverse Event
WARSAW ORTHOPEDIC, INC.·Product code KWP·May 20, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
WARSAW ORTHOPEDIC, INC.·Product code KWP·May 20, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
WARSAW ORTHOPEDIC, INC.·Product code KWP·May 20, 2011
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·February 28, 2013
ASR UNI FEMORAL IMPL SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 28, 2011
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 6, 2014