LANMAGE Ultrasound Diagnostic Scanner - Indonesia BPOM Medical Device Registration
LANMAGE Ultrasound Diagnostic Scanner is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501027605. The device is manufactured by SHENZHEN LANMAGE MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is JEMA INDO MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN LANMAGE MEDICAL TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
JEMA INDO MANDIRIAR Address
Jl. R.S Fatmawati No.100 E, RT 001/RW 009 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selatan, DKI Jakarta - 12430
Registration Date
Dec 05, 2024
Expiry Date
Dec 31, 2028
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
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