10,000 results
·
47ms
·
Sources: EU EUDAMED, US FDA
PURE
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730003515·PURE® Edgewise 018 U/L R/L 3 Rx 0º Tor. 0º Ang....
PURE
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730003928·PURE® Edgewise 022 U/L R/L 3 Rx 0º Tor. 0º Ang....
PURE
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730003553·PURE® Edgewise 018 L R/L 1/2 Rx 0º Tor. 0º Ang....
PURE
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730003966·PURE® Edgewise 022 L R/L 1/2 Rx 0º Tor. 0º Ang....
1.7 RX Turbo-Elite
FDA registration
Terumo BCT STERILIZATION SERVICES, Inc.·1 product·🇺🇸 United States
417-152 1.7 OTW TURBO ELITE
FDA registration
Sterigenics U.S., LLC·1 product·🇺🇸 United States
Device, Incontinence, Mechanical/Hydraulic
FDA Pre-Market Approval
FDA Class 3
·AMS 800 Urinary Control System with and without Inhibizone
ARx MIS Spinal Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
ARx Illiac Spinal Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
ARx® SAI Implant System
FDA 510(k)
FDA Class 2
·Orthopedic
XXXL ARX Liga Spring
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
XXL ARX Liga Spring
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
XL ARX Liga Spring
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
L ARX Liga Spring
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
M ARX Liga Spring
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
S ARX Liga Spring
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
XS ARX Liga Spring
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
XXL ARX Patella Luxation
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
XL ARX Patella Luxation
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market
L ARX Patella Luxation
Device
EU MDR
·
Eu Md Class 1
·Mediroyal Nordic AB·On the market