SIEMENS N Antiserum to Human IgM - Indonesia BPOM Medical Device Registration
SIEMENS N Antiserum to Human IgM is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305220148. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH.Country of Origin
Germany
Authorized Representative
SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Jan 22, 2024
Expiry Date
Oct 19, 2026
Product Type
Immunological Test System
Immunoglobulins A, G, M, D, and E immunological test system.
Invitro Diagnostics
N Antiserum Human Albumin
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