BLT Patient Monitor - Indonesia BPOM Medical Device Registration
BLT Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501127627. The device is manufactured by GUANGDONG BIOLIGHT MEDITECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HOSPI MEDIK INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGDONG BIOLIGHT MEDITECH CO., LTD.Country of Origin
China
Authorized Representative
PT. HOSPI MEDIK INDONESIAAR Address
Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520
Registration Date
Jan 24, 2022
Expiry Date
Sep 18, 2026
Product Type
Diagnostic Cardiology Equipment
Arrhythmia detector and alarm (including ST-segment measurement and alarm).
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