NIPRO GM-30 Inflation Device - Indonesia BPOM Medical Device Registration
NIPRO GM-30 Inflation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501220018. The device is manufactured by GOODMAN CO., LTD. GOODMAN RESEARCH CENTER from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MAKO DUA MEDIKAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GOODMAN CO., LTD. GOODMAN RESEARCH CENTERCountry of Origin
Japan
Authorized Representative
MAKO DUA MEDIKALAR Address
Rukan Avenue 8 No. 125 dan 127 lantai 1, Jakarta Garden City, Kel. Cakung Timur, Kec. Cakung, Kota Jakarta Timur, Provinsi DKI Jakarta, Kode Pos: 13910
Registration Date
Mar 20, 2024
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Cardiology Equipment
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