10,000 results
·
55ms
·
Sources: EU EUDAMED, US FDA
EliA GBM Well
FDA UDI
Phadia AB·07333066014630·EliA GBM Well
GBM P KDY Test(L) 48
FDA UDI
SCIMEDX CORPORATION·00813545022938·
P KDY Pack 4 WELL
FDA UDI
SCIMEDX CORPORATION·00813545020583·
P KDY Pack 8 WELL
FDA UDI
SCIMEDX CORPORATION·00813545020606·
SEEKER™
FDA UDI
BAEBIES, INC.·00819704020081·SEEKER™ GAA Reagent (alpha-D-glucosidase)
GBM P KDY Test(L) 96
FDA UDI
SCIMEDX CORPORATION·00813545022945·
Trinity Biotech
FDA UDI
MARDX DIAGNOSTICS, INC.·05391516748001·Glomerular Basement Membrane IFA Test System, 4...
Trinity Biotech
FDA UDI
MARDX DIAGNOSTICS, INC.·05391516748018·GBM Positive Control, 0.5 mL
Autostat II Anti-GBM
FDA UDI
HYCOR BIOMEDICAL LLC·00816879020137·96 well ELISA for the detection of anti-GBM ant...
QUANTA Flash® GBM Reagents
FDA UDI
INOVA DIAGNOSTICS, INC.·08426950584650·1. 1 QUANTA Flash GBM Reagent Cartridge
VIET NAM ARGENT OPTICAL LIMITED COMPANY
FDA registration
VIET NAM ARGENT OPTICAL LIMITED COMPANY·1 product·🇻🇳 Vietnam
VIET NAM ARGENT OPTICAL LIMITED COMPANY
FDA registration
VIET NAM ARGENT OPTICAL LIMITED COMPANY·1 product·🇻🇳 Vietnam
VIET NAM ARGENT OPTICAL LIMITED COMPANY
FDA registration
VIET NAM ARGENT OPTICAL LIMITED COMPANY·1 product·🇻🇳 Vietnam
ARTIIKA EYEWEAR
FDA registration
VIET NAM ARGENT OPTICAL LIMITED COMPANY·1 product·🇻🇳 Vietnam
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart G5 AED
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart G5 AED
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·Powerheart G5 AED
Dental Zirconia Block
Device
EU MDD
·
Eu Md Class 2a
·Shenzhen Yurucheng Dental Materials Co., Ltd.·On the market·2 countries
VARIOUS GENERAL PURPOSE IVD INSTRUMENTS - IVD MEDICAL DEVICE SOFTWARE
Device
EU IVDD
·
Eu Ivd General
·Sansure Biotech Inc.·On the market
ALTEAFLU Family ES
Device
EU MDD
·
Eu Md Class 2a
·Labomar S.p.A.·On the market·1 country