10,000 results · 51ms · 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