Pure Global

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

TERUMO Preza-Pak II Arterial Blood Sampling Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101918095. 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.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
TERUMO Preza-Pak II Arterial Blood Sampling Kit
Analysis ID: AKL 20101918095

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

Jun 22, 2024

Expiry Date

Apr 10, 2029

Product Type

Diagnostic Anesthesia Equipment

Arterial blood sampling kit.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing