ALINITY i Multi-Assay Manual Diluent - Indonesia BPOM Medical Device Registration
ALINITY i Multi-Assay Manual Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208127839. The device is manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ABBOTT IRELAND DIAGNOSTICS DIVISIONCountry of Origin
Ireland
Authorized Representative
PT. ABBOTT PRODUCTS INDONESIAAR Address
WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA
Registration Date
Oct 25, 2021
Expiry Date
Apr 20, 2026
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
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