OvaCis Rapid Test - Indonesia BPOM Medical Device Registration
OvaCis Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305420264. The device is manufactured by MP BIOMEDICALS ASIA PACIFIC PTE., LTD. from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRITRA PRIMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MP BIOMEDICALS ASIA PACIFIC PTE., LTD.Country of Origin
Singapore
Authorized Representative
TRITRA PRIMA INDONESIAAR Address
Central Park Cikarang Blok A1 No. 02
Registration Date
Jun 07, 2024
Expiry Date
Nov 29, 2028
Product Type
Immunological Test System
Haptoglobin immunological test system.
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