LEICA Surgipath™ Decalcifier II - Indonesia BPOM Medical Device Registration
LEICA Surgipath™ Decalcifier II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204420198. The device is manufactured by LEICA BIOSYSTEMS RICHMOND, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIOGEN SCIENTIFIC.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LEICA BIOSYSTEMS RICHMOND, 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
Sep 03, 2024
Expiry Date
Jun 30, 2025
Product Type
Reagents and Specimen Providers
General purpose reagent.
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