ORTHO BLISS - Indonesia BPOM Medical Device Registration
ORTHO BLISS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420295. The device is manufactured by MILLIPORE UK LTD. UNITED KINGDOM from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DIASTIKA BIOTEKINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MILLIPORE UK LTD. UNITED KINGDOMCountry of Origin
United Kingdom
Authorized Representative
DIASTIKA BIOTEKINDOAR Address
Rukan Sentra Pemuda Kav.30 - 31 Jalan Pemuda No.61 RT.009 RW.003 Kel. Rawamangun Kec.Pulogadung
Registration Date
Jul 30, 2024
Expiry Date
Feb 15, 2027
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Potentiating media for in vitro diagnostic use.
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