OMNILINK ELITE Peripheral Stent System - Indonesia BPOM Medical Device Registration
OMNILINK ELITE Peripheral Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503516313. The device is manufactured by ABBOTT VASCULAR from Ireland, 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
Ireland
Authorized Representative
PT. ABBOTT PRODUCTS INDONESIAAR Address
WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA
Registration Date
Apr 01, 2020
Expiry Date
Dec 31, 2025
Product Type
Prosthetic Cardiology Equipment
Coronary stent
Non Electromedic Sterile
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