YESON AUTOCLAVE - Indonesia BPOM Medical Device Registration
YESON AUTOCLAVE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903913383. The device is manufactured by NINGBO HAISHU YESON MEDICAL DEVICE CO. LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MANDALA MITRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NINGBO HAISHU YESON MEDICAL DEVICE CO. LTDCountry of Origin
China
Authorized Representative
PT. MANDALA MITRATAMAAR Address
Komplek Ruko Roxy Mas Blok C 2 No. 12 Jl. Hasyim Ashari 125
Registration Date
Jun 01, 2023
Expiry Date
Apr 03, 2028
Product Type
General Hospital Equipment and Other Individuals
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