JEOL Reference Electrode - Indonesia BPOM Medical Device Registration
JEOL Reference Electrode is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322490. The device is manufactured by JEOL YAMAGATA CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SYSMEX INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JEOL YAMAGATA CO., LTD.Country of Origin
Japan
Authorized Representative
PT. SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Nov 06, 2024
Expiry Date
Jul 05, 2026
Product Type
Clinical Chemistry Test System
Multi parameter clinical chemistry test system
Invitro Diagnostics
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