GRIP RX PTCA Catheter - Indonesia BPOM Medical Device Registration
GRIP RX PTCA Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501611068. The device is manufactured by ACROSTAK (SCHWEIZ) AG from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HARMONI PRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACROSTAK (SCHWEIZ) AGCountry of Origin
Switzerland
Authorized Representative
PT. HARMONI PRIMA MEDIKAAR Address
Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150
Registration Date
Jan 12, 2022
Expiry Date
Aug 26, 2026
Product Type
Diagnostic Cardiology Equipment
Percutaneous catheter.
Non Electromedic Sterile
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