RANDOX RX Series CK-MB - Indonesia BPOM Medical Device Registration
RANDOX RX Series CK-MB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220215. The device is manufactured by RANDOX LABORATORIES LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TAMARA OVERSEAS CORPORINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RANDOX LABORATORIES LTD.Country of Origin
United Kingdom
Authorized Representative
PT. TAMARA OVERSEAS CORPORINDOAR Address
Jl. Pinangsia Timur No. 49 Jakarta 11110
Registration Date
Feb 22, 2022
Expiry Date
Nov 09, 2025
Product Type
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