NIHON PER Hemolynac - 510 - Indonesia BPOM Medical Device Registration
NIHON PER Hemolynac - 510 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208911016. The device is manufactured by NIHON KOHDEN TOMIOKA CORPORATION. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GANDASARI EKASATYA.
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NIHON KOHDEN Hemolynac - 510
Risk Classification
Product Class
Kelas : 2
Manufacturer
NIHON KOHDEN TOMIOKA CORPORATION.Country of Origin
Japan
Authorized Representative
PT. GANDASARI EKASATYAAR Address
Jl. Raya Mabes Hankam No.5 9A, RT.7/RW.2
Registration Date
Nov 11, 2024
Expiry Date
May 30, 2026
Product Type
Hematological Reagents
Red cell lysing reagent.
Invitro Diagnostics
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