HeRO Graft - Indonesia BPOM Medical Device Registration
HeRO Graft is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503917829. The device is manufactured by MERIT MEDICAL SYSTEMS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PERMATA MEDIKA PRIMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MERIT MEDICAL SYSTEMS, INC.Country of Origin
United States
Authorized Representative
PT. PERMATA MEDIKA PRIMAAR Address
JL. HOS COKROAMINOTO, PERTOKOAN CBD CILEDUG BLOK A3 NO. 30, RT.001/RW.001
Registration Date
Jun 23, 2023
Expiry Date
Dec 31, 2025
Product Type
Prosthetic Cardiology Equipment
Vascular graft prosthesis
Non Electromedic Sterile
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