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FOCUS Lipase (LPS/Methyl halogen test) - Indonesia BPOM Medical Device Registration

FOCUS Lipase (LPS/Methyl halogen test) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221393. The device is manufactured by SHENZEN ICUBIO BIOMEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
FOCUS Lipase (LPS/Methyl halogen test)

FOKUS Lipase (LPS/Methyl test halogen)

Analysis ID: AKL 20101221393

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FOCUS DIAGNOSTIC INDONESIA

AR Address

18 Office Park, Tower A, Jl. TB Simatupang No.18 MZ Floor, Unit D1-A/89, Kelurahan Kebagusan

Registration Date

Aug 30, 2022

Expiry Date

Aug 30, 2025

Product Type

Clinical Chemistry Test System

Lipase test system (kit & cair)

Invitro Diagnostics

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