SYSMEX Lysercell WDF II - Indonesia BPOM Medical Device Registration
SYSMEX Lysercell WDF II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420067. The device is manufactured by SYSMEX CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is Sysmex Indonesia.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
SYSMEX CORPORATIONCountry of Origin
Japan
Authorized Representative
Sysmex IndonesiaAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Apr 16, 2024
Expiry Date
Dec 07, 2028
Product Type
Hematological Reagents
Red cell lysing reagent.
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