BIOTA VA-360L LYSE - Indonesia BPOM Medical Device Registration
BIOTA VA-360L LYSE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208022863. The device is manufactured by BIOTA GRUP SAGLIK SI STEMLERI SAN. VE ICT. LTD. STI. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. CIPTA VARIA KHARISMA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
PT. CIPTA VARIA KHARISMA UTAMAAR Address
Jl. Utan Kayu Raya No. 105A Jakarta
Registration Date
Mar 28, 2023
Expiry Date
Mar 08, 2028
Product Type
Hematological Reagents
Red cell lysing reagent.
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