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NeuMoDx EBV External Controls - Indonesia BPOM Medical Device Registration

NeuMoDx EBV External Controls is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303124355. The device is manufactured by NEUMODX MOLECULAR, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INODIA.

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 : C
NeuMoDx EBV External Controls
Analysis ID: AKL 20303124355

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

INODIA

AR Address

Perkantoran Kedoya Elok Plaza Blok DB no 24, Jalan Panjang, Kebon Jeruk

Registration Date

Jul 24, 2021

Expiry Date

Oct 08, 2025

Product Type

Serological Reagents

Epstein-Barr virus serological reagents.

Invitro Diagnostics

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