JUNGSON Centrifuge - Indonesia BPOM Medical Device Registration
JUNGSON Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10209220218. The device is manufactured by ZENITH LAB (JIANGSU) CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PURE SOURCE OF ALKESINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ZENITH LAB (JIANGSU) CO.,LTDCountry of Origin
China
Authorized Representative
PT. PURE SOURCE OF ALKESINDOAR Address
KOMP. PERGUDANGAN PRIMA CENTER 1 EXTENSION F NO 36
Registration Date
Oct 03, 2022
Expiry Date
Oct 02, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Blood bank centrifuge for in vitro diagnostic use.
Invitro Diagnostics
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