IRADIMED MRIDIUM MRI Infusion Pump / Monitoring System - Indonesia BPOM Medical Device Registration
IRADIMED MRIDIUM MRI Infusion Pump / Monitoring System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420869. The device is manufactured by IRADIMED CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTIMEDIKA PUSPA INDAH.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
IRADIMED CORPORATION.Country of Origin
United States
Authorized Representative
PT. INTIMEDIKA PUSPA INDAHAR Address
JL Gading Kirana Utara Blok E 10 No 32 Kelapa Gading Barat,Kelapa Gading Jakarta Utara
Registration Date
Aug 19, 2024
Expiry Date
May 27, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Infusion pump.
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