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INZONE Detachment System - Indonesia BPOM Medical Device Registration

INZONE Detachment System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003420020. The device is manufactured by BENCHMARK ELECTRONICS, INC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. NUGRA KARSERA.

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 : D
INZONE Detachment System
Analysis ID: AKL 31003420020

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

Authorized Representative

PT. NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Mar 01, 2024

Expiry Date

Jun 30, 2025

Product Type

Therapeutic Neurology Equipment

Neurovascular embolization device.

Non Radiation Electromedics

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