MOSAIQ Sample Diluent 2 - Indonesia BPOM Medical Device Registration
MOSAIQ Sample Diluent 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101421959. The device is manufactured by ALBA BIOSCIENCE LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ALBA BIOSCIENCE LTD.Country of Origin
United Kingdom
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 07, 2024
Expiry Date
May 28, 2029
Product Type
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