LMB FILTRAmatic - Indonesia BPOM Medical Device Registration
LMB FILTRAmatic is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209817592. The device is manufactured by LMB TECHNOLOGIE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FRISMED HOSLAB INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LMB TECHNOLOGIE GMBH.Country of Origin
Germany
Authorized Representative
PT. FRISMED HOSLAB INDONESIAAR Address
Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321
Registration Date
Sep 11, 2024
Expiry Date
Jan 01, 2029
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood cell separator
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