ARIA Perfect AV Fistula - Indonesia BPOM Medical Device Registration
ARIA Perfect AV Fistula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320794. The device is manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. WORCKHARDT PHARMA INDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HOSPITECH MANUFACTURING SERVICES SDN. BHD.Country of Origin
Malaysia
Authorized Representative
PT. WORCKHARDT PHARMA INDOAR Address
RUKAN GRAHA CEMPAKA MAS BLOK D-19, JL. LETNAN JENDRAL SUPRAPTO
Registration Date
Jun 16, 2023
Expiry Date
Jun 15, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
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