NKMAX NK VUE Kit - Indonesia BPOM Medical Device Registration
NKMAX NK VUE Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306718714. The device is manufactured by NKMAX CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDISON JAYA RAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NKMAX CO., LTD.Country of Origin
Korea
Authorized Representative
MEDISON JAYA RAYAAR Address
JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN
Registration Date
Apr 21, 2021
Expiry Date
Sep 08, 2024
Product Type
Tumor Antigen Immunologic Test System
Immunomagnetic circulating cancer cell selection and enumeration system.
Invitro Diagnostics
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