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CDI Blood Parameter Monitoring System 550 - Indonesia BPOM Medical Device Registration

CDI Blood Parameter Monitoring System 550 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501914761. The device is manufactured by TERUMO CARDIOVASCULAR SYSTEMS CORP. from United States, 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.

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BPOM Registered
Risk Class Kelas Resiko : B
CDI Blood Parameter Monitoring System 550
Analysis ID: AKL 20501914761

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. TERUMO INDONESIA

AR Address

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

Registration Date

Nov 17, 2023

Expiry Date

Oct 04, 2028

Product Type

Diagnostic Cardiology Equipment

Blood pressure computer.

Non Radiation Electromedics

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