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MEDRAD Centargo Replacement Spike - Indonesia BPOM Medical Device Registration

MEDRAD Centargo Replacement Spike is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501128005. The device is manufactured by B.BRAUN AVITUM ITALY from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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
MEDRAD Centargo Replacement Spike
Analysis ID: AKL 20501128005

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

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

Dec 17, 2021

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Cardiology Equipment

Angiographic injector and syringe.

Non Electromedic Sterile

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