JMS Infusion Pump - Indonesia BPOM Medical Device Registration
JMS Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902713882. The device is manufactured by MED-TECH INC. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is KARINDO ALKESTRON.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MED-TECH INC.Country of Origin
Japan
Authorized Representative
KARINDO ALKESTRONAR Address
JL. TOMANG RAYA NO.17
Registration Date
Jan 28, 2021
Expiry Date
Sep 17, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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