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EZ1 Advanced XL - Indonesia BPOM Medical Device Registration

EZ1 Advanced XL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10102710254. The device is manufactured by QIAGEN GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. 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
EZ1 Advanced XL
Analysis ID: AKL 10102710254

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

QIAGEN GMBH.

Country of Origin

Germany

Authorized Representative

PT. INODIA

AR Address

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

Registration Date

Nov 06, 2020

Expiry Date

Nov 27, 2024

Product Type

Immunology Laboratory Equipment and Reagents

RNA Preanalytical Systems.

Invitro Diagnostics

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