BRIGHTWAY HOLDINGS SDN. BHD.

FDA registration

BRIGHTWAY HOLDINGS SDN. BHD.·1 product·🇲🇾 Malaysia

STERILE BRIGHTWAY BRAND POWER-FREE, LATEX EXAMINATION GLOVES, WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS) TESTED

FDA 510(k)

FDA Class 1 ·General Hospital

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·04051526743632·LEVAMED ANKLE SUPPORT SAND VI

Tissue Expander Hemisphere 2ml

FDA registration

FCI SUD·1 product·🇲🇺 Mauritius

Dento Prep

FDA registration

RONVIG DENTAL MFG. A/S·1 product·🇩🇰 Denmark

Tissue Expander Hemisphere 2ml

FDA registration

FCI FRANCE CHIRURGIE INSTRUMENTATION·1 product·🇫🇷 France

Tissue Expander Hemisphere 2ml

FDA registration

FCI SAS·1 product·🇫🇷 France

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450265741·

NTI-tss

FDA registration

Boyd Research·1 product·🇺🇸 United States

R108F

FDA registration

RALCO S.R.L.·1 product·🇮🇹 Italy

SUPERCROSS CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

UTERINE MANIPULATOR INJECTOR CANNULA, STERILE, MODEL R 57-450

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Cannula, Manipulator/Injector, Uterine

FDA classification

FDA Class 2 ·Cannula, Manipulator/Injector, Uterine

Latex Patient Examination Glove

FDA classification

FDA Class 1 ·Latex Patient Examination Glove

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous