DIAGON Dia-FIB - Indonesia BPOM Medical Device Registration
DIAGON Dia-FIB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207900021. The device is manufactured by DIAGON LTD. from Hungary, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIAGONTAMA CORE ALIGNED.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAGON LTD.Country of Origin
Hungary
Authorized Representative
PT. DIAGONTAMA CORE ALIGNEDAR Address
Perkantoran Plaza Pasifik Blok A3/59 Jl. Raya Boulevard barat, Kelapa Gading - Jakarta Utara Telp : 021-45840649-45840650
Registration Date
Feb 18, 2019
Expiry Date
Nov 23, 2023
Product Type
Haematology Package and Kit
Fibrinogen determination system.
Invitro Diagnostics
