HI-TORQUE Extra S'port Guide Wire - Indonesia BPOM Medical Device Registration
HI-TORQUE Extra S'port Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501611246. 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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HI-TORQUE Extra S’port Guide Wire
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
Nov 05, 2019
Expiry Date
Apr 17, 2024
Product Type
Diagnostic Cardiology Equipment
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