JMS Syringe Pump - Indonesia BPOM Medical Device Registration
JMS Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902713839. The device is manufactured by JMS CO., LTD. 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
JMS CO., LTD.Country of Origin
Japan
Authorized Representative
KARINDO ALKESTRONAR Address
JL. TOMANG RAYA NO.17
Registration Date
Mar 03, 2021
Expiry Date
Sep 17, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
Non Radiation Electromedics
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