SWELAB Snow-D Diluent - Indonesia BPOM Medical Device Registration
SWELAB Snow-D Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208914016. The device is manufactured by BOULE MEDICAL. from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NARWASTU MEDIKA.
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SWELAB Lumi-D Diluent
Risk Classification
Product Class
Kelas : 2
Manufacturer
BOULE MEDICAL.Country of Origin
Sweden
Authorized Representative
PT. NARWASTU MEDIKAAR Address
Jl. Daan Mogot km.20 No.411A Kelurahan Kebon Besar
Registration Date
Mar 15, 2024
Expiry Date
Feb 08, 2027
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
SWELAB Lumi L1-Lyse
LUMILAB BOULE Cal-5Diff A1
SWELAB Lumi and Accessories
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