ELECSYS HCG+β - Indonesia BPOM Medical Device Registration
ELECSYS HCG+β is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101422491. The device is manufactured by ROCHE DIAGNOSTICS (SUZHOU) LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ROCHE INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ROCHE DIAGNOSTICS (SUZHOU) LTDCountry of Origin
China
Authorized Representative
PT. ROCHE INDONESIAAR Address
Gedung AIA Central Lantai 36 Jl. Jend. Sudirman KAV. 48A RT/RW 003/004 Kelurahan Karet Semanggi
Registration Date
Dec 06, 2024
Expiry Date
Sep 04, 2029
Product Type
Clinical Chemistry Test System
Human chorionic gonadotropin (HCG) test system (kit & cair)
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