INFOMED Blood Purification Devices - Indonesia BPOM Medical Device Registration
INFOMED Blood Purification Devices is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420525. The device is manufactured by INFOMED SA from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INFOMED SACountry of Origin
Switzerland
Authorized Representative
TRANSMEDIC INDONESIAAR Address
Perkantoran Menara Era Unit G-01 JL.Senen Raya No.135-137 RT 00 RW 00, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Senen, Kel. Senen
Registration Date
Oct 15, 2024
Expiry Date
Jun 22, 2029
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
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