18 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SELF CATH SET/SAFETY CATH
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
APC/Fire™ 750 anti-human CD45RA
FDA UDI
BIOLEGEND, INC.·00810034702296·URL: https://www.biolegend.com/en-us/products/a...
Polystar Selection EDITION HD
FDA UDI
Merz Dental GmbH·D7091983010·posteriors; shade A2; size L; upper jaw
9830-10 Sensor
FDA UDI
Tekscan, Inc.·B9709830100·9830-10 Sensor
Skipjack
FDA UDI
Seaspine Orthopedics Corporation·10889981138882·Slap Hammer
Tronex International, Inc.
FDA UDI
TRONEX INTERNATIONAL, INC.·10097604983010·Glove, Exam, Nitrile, Chemotherapy Rated, Finge...
SHENZHEN MED-LINKET ADULT FINGER CLIP SPO2 SENSOR, SHENZHEN MED-LINKET ADULT SILICONE SOFT TIP SPO2 SENSOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Smith & Nephew VISIONAIRE Patient Matched Cutting Blocks
FDA 510(k)
FDA Class 2
·Orthopedic
PINN CAN BONE SCREW 6.5MMX15MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018
SUMMIT POR TAPER SZ6 STD OFF
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018
PINN CAN BONE SCREW 6.5MMX25MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018
MIS Quad-Sparing™
FDA UDI
Zimmer, Inc.·00889024217959·
ARCHITECT CREATINE KINASE
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018
ARCHITECT CREATINE KINASE
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018
ARCHITECT CREATINE KINASE
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code CGS·July 21, 2018
7.0MM TI PANGEA POLY NAIL
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code NKB·February 26, 2013
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·August 6, 2014
CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code DYE·February 10, 2011