COVIDIEN Clearify Visualization Systems - Indonesia BPOM Medical Device Registration
COVIDIEN Clearify Visualization Systems is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801714155. The device is manufactured by COVIDIEN. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDTRONIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
COVIDIEN.Country of Origin
United States
Authorized Representative
MEDTRONIC INDONESIAAR Address
Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda
Registration Date
Jan 21, 2021
Expiry Date
Oct 21, 2025
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories.
Non Radiation Electromedics
NEWPORT™ e360 Ventilator with Accessories, T Model
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PURITAN BENNETT 560 Ventilator
COVIDIEN Pediatric SomaSensor®
COVIDIEN OxyAlert NIRSensor
COVIDIEN Infant SpO2 Sensor
COVIDIEN NELLCOR Neonatal-Adult SpO2 Sensor
COVIDIEN NELLCOR Adult SpO2 Sensor
COVIDIEN Somanetics Invos Oximeter
COVIDIEN NELLCOR SpO2 Sensor
NG BIO-MEDICUS Pediatric Venous Cannula and Introducers
MEDTRONIC MEXICO S DE R.L DE CV
NG Bio-Medicus Adult Arterial/Internal Jugular Cannula Kits
MEDTRONIC MEXICO S DE R.L DE CV
AFFINITY CP Centrifugal Blood Pump
MEDTRONIC MEXICO S. DE R.L. DE CV
MEDTRONIC Lumboperitonial Shunt
MEDTRONIC DOMINICANA (MANUFACTURA) S.A.
MEDTRONIC CSF Valves And Buttons
MEDTRONIC DOMINICANA (MANUFACTURA) S.A.
MEDTRONIC Ventricular Catheters
MEDTRONIC NEUROSURGERY
MEDTRONIC Shunt Accessories
MEDTRONIC DOMINICANA (MANUFACTURA) S.A.
MEDTRONIC Shunt Kits
MEDTRONIC DOMINICANA (MANUFACTURA) S.A.
MEDTRONIC EDM Lumbar
MEDTRONIC MEXICO S. DE R.L. DE CV
CG Future Sizer Sets
MEDTRONIC HEART VALVE DIVISION