LEICA Aperio GT 450 DX and Accessories - Indonesia BPOM Medical Device Registration
LEICA Aperio GT 450 DX and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20203220098. The device is manufactured by LEICA BIOSYSTEMS IMAGING, INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOGEN SCIENTIFIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LEICA BIOSYSTEMS IMAGING, INCCountry of Origin
United States
Authorized Representative
PT. BIOGEN SCIENTIFICAR Address
Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21 RT.002/RW.001 Tanjung Barat, Jagakarsa, Jakarta Selatan, DKI Jakarta
Registration Date
Dec 16, 2024
Expiry Date
Jun 30, 2026
Product Type
Pathology Equipment and Accessories
Whole slide imaging system
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