BIOSYSTEMS FIBRINOGEN - Indonesia BPOM Medical Device Registration
BIOSYSTEMS FIBRINOGEN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207320332. The device is manufactured by BIOSYSTEMS S.A. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ELGA TAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOSYSTEMS S.A.Country of Origin
Spain
Authorized Representative
PT. ELGA TAMAAR Address
JL. RASAMALA RAYA NO. 12 D RT. 006 RW. 003 KELURAHAN JATIPULO, KECAMATAN PALMERAH
Registration Date
Jun 16, 2023
Expiry Date
Dec 24, 2025
Product Type
Haematology Package and Kit
Fibrinogen determination system.
Invitro Diagnostics
BIOSYSTEMS RHEUMATOID FACTORS (RF) STANDARD
BIOSYSTEMS APOLIPOPROTEIN B (APO B)
BIOSYSTEMS CARBON DIOXIDE (CO2)
BIOSYSTEMS Homocysteine Standards
BIOSYSTEMS SEROLOGY NEGATIVE CONTROL
BIOSYSTEMS FIBRINOGEN CONTROL PLASMA
BIOSYSTEMS APOLIPOPROTEIN B (APO B) STANDARD
BIOSYSTEMS HOMOCYSTEINE CONTROL II
BIOSYSTEMS CK-MB CONTROL SERUM II
BIOSYSTEMS HOMOCYSTEINE CONTROL I
BIOSYSTEMS RHEUMATOID FACTORS (RF) STANDARD
BIOSYSTEMS S.A.
BIOSYSTEMS Homocysteine Standards
BIOSYSTEMS S.A.
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