ANSCARE CHITOCLOT Artery Femoral Compression Device - Indonesia BPOM Medical Device Registration
ANSCARE CHITOCLOT Artery Femoral Compression Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504810009. The device is manufactured by BENQ MATERIALS CORPORATION TAOYUAN FACTORY from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN REVASS MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BENQ MATERIALS CORPORATION TAOYUAN FACTORYCountry of Origin
Taiwan (China)
Authorized Representative
PT. MAIN REVASS MEDIKAAR Address
Jl. Dewi Sartika No. 4B RT 004/007 Kel. Cililitan Kec. Kramat jati
Registration Date
Apr 29, 2024
Expiry Date
Dec 29, 2026
Product Type
Surgical Cardiology Equipment
Vascular clamp.
Non Electromedic Sterile
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