CREO MY Instrument - Indonesia BPOM Medical Device Registration
CREO MY Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303125717. The device is manufactured by GLOBUS MEDICAL, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ASIA ACTUAL INDONESIA.
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CREO MIS Instrument
Risk Classification
Product Class
Kelas : 1
Manufacturer
GLOBUS MEDICAL, INC.Country of Origin
United States
Authorized Representative
ASIA ACTUAL INDONESIAAR Address
PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN
Registration Date
Sep 15, 2021
Expiry Date
Jan 08, 2025
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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