REMEL Coagulase Plasma - Indonesia BPOM Medical Device Registration
REMEL Coagulase Plasma is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20302913993. The device is manufactured by REMEL INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIPA PUSPA LABSAINS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
REMEL INC.Country of Origin
United States
Authorized Representative
PT. DIPA PUSPA LABSAINSAR Address
Dipa Strategic Office, Lantai Lobby, Jl. Raya Kebayoran Lama No.28 RT.009/RW.011, Kel. Grogol Utara, Kec. Kebayoran Lama
Registration Date
Dec 26, 2022
Expiry Date
Oct 05, 2025
Product Type
Microbiology Equipment
Coagulase plasma.
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