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HOKAPI™ CUVETTE - Indonesia BPOM Medical Device Registration

HOKAPI™ CUVETTE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520224. The device is manufactured by SUZHOU HOKAPI BIOMEDICAL ENGINEERING CO., LTD 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
HOKAPI™ CUVETTE
Analysis ID: AKL 20101520224

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

Feb 01, 2025

Expiry Date

Dec 31, 2025

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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