NEOMEDICA Neo Diluent C - Indonesia BPOM Medical Device Registration
NEOMEDICA Neo Diluent C is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320616. The device is manufactured by NEOMEDICA D.O.O. from Serbia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ELGA TAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NEOMEDICA D.O.O.Country of Origin
Serbia
Authorized Representative
ELGA TAMAAR Address
JL. RASAMALA RAYA NO. 12 D RT. 006 RW. 003 KELURAHAN JATIPULO, KECAMATAN PALMERAH
Registration Date
Jun 07, 2024
Expiry Date
Mar 29, 2027
Product Type
Hematological Reagents
Blood cell diluents
Invitro Diagnostics
BIOSYSTEMS CARBON DIOXIDE (CO2)
BIOSYSTEMS S.A.
BIOSYSTEMS APOLIPOPROTEIN B (APO B)
BIOSYSTEMS S.A.
BIOSYSTEMS SEROLOGY NEGATIVE CONTROL
BIOSYSTEMS S.A.
NEOMEDICA Neo U Stain
NEOMEDICA DOO
BIOSYSTEMS Activated Partial Thromboplastin Time (APTT)
BIOSYSTEMS S.A.
BIOSYSTEMS Fibrinogen Clauss
BIOSYSTEMS S.A.
BIOSYSTEMS Cholesterol HDL Direct
BIOSYSTEMS S.A.
BIOSYSTEMS Total Bile Acids
BIOSYSTEMS S.A.
BIOSYSTEMS AMMONIA, ETHANOL, CO2 CONTROL I
BIOSYSTEMS S.A.
BIOSYSTEMS Oxalate
BIOSYSTEMS S.A.