HEMONART BlacT ACT TEST TUBE - Indonesia BPOM Medical Device Registration
HEMONART BlacT ACT TEST TUBE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207320447. The device is manufactured by HEMONART MEDICAL SYSTEMS INDUSTRY TRADE JOINT STOCK COMPANY from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BINTANG MONO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
BINTANG MONO INDONESIAAR Address
Perum Mahkota Simprug Blok A13 No. 9
Registration Date
Nov 14, 2023
Expiry Date
Jan 16, 2028
Product Type
Haematology Package and Kit
Activated whole blood clotting time tests.
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