ARJOHUNTLEIGH Maxi Move - Indonesia BPOM Medical Device Registration
ARJOHUNTLEIGH Maxi Move is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903914779. The device is manufactured by ARJOHUNTLEIGH MAGOG INC. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTERGASTRA NUSANTARA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ARJOHUNTLEIGH MAGOG INC.Country of Origin
Canada
Authorized Representative
PT. INTERGASTRA NUSANTARAAR Address
Pangeran Jayakarta 24/34-35 Mangga Dua Selatan Sawah Besar- Jakarta Pusat
Registration Date
Dec 27, 2022
Expiry Date
Dec 31, 2025
Product Type
General Hospital Equipment and Other Individuals
Powered patient transfer device.
Non Radiation Electromedics
ELMASONIC Med
ELMA SCHMIDBAEUR GMBH.
ELMASONIC Med
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ELMASONIC Med
ELMA SCHMIDBAEUR GMBH.
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