IMMULITE1000 Rubella IgM - Indonesia BPOM Medical Device Registration
IMMULITE1000 Rubella IgM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220110. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTDCountry of Origin
United Kingdom
Authorized Representative
SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Feb 25, 2022
Expiry Date
Jan 24, 2025
Product Type
Serological Reagents
Rubella virus serological reagents.
Invitro Diagnostics
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