RANDOX RX series Mg (Magnesium) - Indonesia BPOM Medical Device Registration
RANDOX RX series Mg (Magnesium) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322663. 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 TAMARA OVERSEAS CORPORINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RANDOX LABORATORIES, LTDCountry of Origin
United Kingdom
Authorized Representative
TAMARA OVERSEAS CORPORINDOAR Address
Jl. Pinangsia Timur No. 49 Jakarta 11110
Registration Date
Feb 23, 2023
Expiry Date
Nov 09, 2025
Product Type
Clinical Chemistry Test System
Magnesium test system (kit & cair)
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