RGC™ - Revass Guiding Catheter - Indonesia BPOM Medical Device Registration
RGC™ - Revass Guiding Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501911630. The device is manufactured by APT MEDICAL INC. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN REVASS MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
APT MEDICAL INC.Country of Origin
China
Authorized Representative
PT. MAIN REVASS MEDIKAAR Address
Jl. Dewi Sartika No. 4B RT 004/007 Kel. Cililitan Kec. Kramat jati
Registration Date
Apr 18, 2022
Expiry Date
Dec 31, 2024
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
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