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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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BPOM Registered
Risk Class Kelas Resiko : B
NKMAX NK VUE Kit
Analysis ID: AKL 20306718714

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

NKMAX CO., LTD.

Country of Origin

Korea

Authorized Representative

MEDISON JAYA RAYA

AR 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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