SUPERA Peripheral Stent System - Indonesia BPOM Medical Device Registration
SUPERA Peripheral Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503520008. The device is manufactured by ABBOTT VASCULAR from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ABBOTT VASCULARCountry of Origin
United States
Authorized Representative
PT. ABBOTT PRODUCTS INDONESIAAR Address
Wisma Pondok Indah 2, Suite 1000, Jl. Sultan Iskandar Muda Kav V - TA
Registration Date
Jan 23, 2025
Expiry Date
Sep 11, 2025
Product Type
Prosthetic Cardiology Equipment
Peripheral Stent (cardiovascular use)
Non Electromedic Sterile
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