HI-TORQUE WHISPER Guide Wire - Indonesia BPOM Medical Device Registration
HI-TORQUE WHISPER Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501611245. The device is manufactured by ABBOTT VASCULAR. from Puerto Rico USA, 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 VASCULAR.Country of Origin
Puerto Rico USA
Authorized Representative
PT. ABBOTT PRODUCTS INDONESIAAR Address
WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA
Registration Date
Sep 01, 2022
Expiry Date
Apr 17, 2024
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
Non Electromedic Sterile
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