X.ACT Carotid Stent System - Indonesia BPOM Medical Device Registration
X.ACT Carotid Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003611477. The device is manufactured by ABBOTT VASCULAR from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.
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Risk Classification
Product Class
Kelas : 3
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
Nov 06, 2024
Expiry Date
Jan 30, 2029
Product Type
Therapeutic Neurology Equipment
Carotid stent
Non Electromedic Sterile
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