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ELVASENSE ORIGIN - Indonesia BPOM Medical Device Registration

ELVASENSE ORIGIN is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101124483. The device is manufactured by PHILOSYS, CO., LTD., from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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BPOM Registered
Risk Class Kelas Resiko : C
ELVASENSE ORIGIN
Analysis ID: AKL 20101124483

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. ENSEVAL MEDIKA PRIMA

AR Address

JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG

Registration Date

Jul 26, 2021

Expiry Date

Jul 08, 2025

Product Type

Clinical Chemistry Test System

Glucose test system

Invitro Diagnostics

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