LEICA Autostainer XL ST5010 and Accessories - Indonesia BPOM Medical Device Registration
LEICA Autostainer XL ST5010 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20203915542. The device is manufactured by LEICA BIOSYSTEMS NUSSLOCH GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BIOGEN SCIENTIFIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LEICA BIOSYSTEMS NUSSLOCH GMBH.Country of Origin
Germany
Authorized Representative
BIOGEN SCIENTIFICAR Address
Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21
Registration Date
Jul 26, 2023
Expiry Date
Jun 30, 2025
Product Type
Pathology Equipment and Accessories
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