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TERUMO Preza Pak II Arterial Blood Sampler - Indonesia BPOM Medical Device Registration

TERUMO Preza Pak II Arterial Blood Sampler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209113431. The device is manufactured by KOFU FACTORY of TERUMO CORPORATION. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TERUMO INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
TERUMO Preza Pak II Arterial Blood Sampler
Analysis ID: AKL 20209113431

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. TERUMO INDONESIA

AR Address

Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta

Registration Date

Oct 27, 2022

Expiry Date

Nov 25, 2026

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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