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ELVASENSE Blood Pressure Monitor - Indonesia BPOM Medical Device Registration

ELVASENSE Blood Pressure Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501026001. The device is manufactured by GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO., LTD, CHINA from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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BPOM Registered
Risk Class Kelas Resiko : B
ELVASENSE Blood Pressure Monitor
Analysis ID: AKL 20501026001

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

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

Sep 15, 2023

Expiry Date

Jul 01, 2026

Product Type

Diagnostic Cardiology Equipment

Noninvasive blood pressure measurement system.

Non Radiation Electromedics

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