HUMAN RUBELLA IgM µ - capture - Indonesia BPOM Medical Device Registration
HUMAN RUBELLA IgM µ - capture is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303022177. The device is manufactured by HUMAN GESELLSCHAFT FÜR BIOCHEMICA UND DIAGNOSTICA MBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SALI POLAPA TOGETHER.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Germany
Authorized Representative
PT. SALI POLAPA TOGETHERAR Address
Puri Sentra Niaga Blok B 33-34 Jl. Raya Kalimalang 13620
Registration Date
Mar 01, 2023
Expiry Date
Dec 31, 2027
Product Type
Serological Reagents
Rubella virus serological reagents.
Invitro Diagnostics
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