ATELLICA IN THE TSTII - Indonesia BPOM Medical Device Registration
ATELLICA IN THE TSTII is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101025289. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC. (EAST WALPOLE) from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.
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ATELLICA IM TSTII
Risk Classification
Product Class
Kelas : 2
Country of Origin
United States
Authorized Representative
PT. 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
Sep 14, 2020
Expiry Date
Mar 04, 2025
Product Type
Clinical Chemistry Test System
Testosterone test system (kit & cair)
Invitro Diagnostics
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