40 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SR1 T3 UPTAKE ENZYME IMMUNOASSAY(MAG SOLID-PHASE)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450201169·
Pinnacle
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730010421·Pinnacle .018 R UR 4/5 HK -7T 0A 2DO (10PK)
Votion
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730008596·Votion .018 R UR 4/5 HK -7T 0A 2DO (10PK)
Votion®
FDA UDI
Ortho Organizers, Inc.·00190707114299·Votion .018 R UR 4/5 HK -7T 0A 2DO (10PK)
Pinnacle®
FDA UDI
Ortho Organizers, Inc.·00190707112387·Pinnacle .018 R UR 4/5 HK -7T 0A 2DO (10PK)
MODEL 2000 AXYALOOP SELF-TAPPING BONE ANCHOR, MODEL 2000
FDA 510(k)
FDA Class 2
·Orthopedic
MOBILETT MIRA
FDA 510(k)
FDA Class 2
·Radiology
InterFuse L
FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010717·Intervertebral Body Fusion Device
InterFuse L
FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010700·Intervertebral Body Fusion Device
InterFuse L
FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010861·Intervertebral Body Fusion Device
InterFuse L
FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010878·Intervertebral Body Fusion Device
InterFuse L
FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010885·Intervertebral Body Fusion Device
InterFuse L
FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010854·Intervertebral Body Fusion Device
InterFuse L
FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010694·Intervertebral Body Fusion Device
InterFuse L
FDA UDI
NEXT ORTHOSURGICAL, INC.·00819475010724·Intervertebral Body Fusion Device
FREELITE HUMAN KAPPA AND HUMAN LAMBDA FREE KITS FOR USE ON THE HITACHI 911/912 ANALYZER
FDA 510(k)
FDA Class 2
·Immunology
HUMAN IGG SUBCLASS LIQUID REAGENT KITS (FOR USE ON HITACHI 911/ 912/ 917 AND MODULAR P)
FDA 510(k)
FDA Class 2
·Immunology
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·November 24, 2010
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code NVY·January 11, 2013