Pure Global

EVO R+ - Indonesia BPOM Medical Device Registration

EVO R+ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220296. The device is manufactured by TECHNIX SPA from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GRATIA JAYA MULYA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
EVO R+
Analysis ID: AKL 21501220296

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

TECHNIX SPA

Country of Origin

Italy

Authorized Representative

PT. GRATIA JAYA MULYA

AR Address

Gading Park View Blok ZC.I No. 10-11 Jl. Boulevard Timur Raya

Registration Date

Jul 05, 2022

Expiry Date

Mar 01, 2027

Product Type

Diagnostic Radiology Equipment

Mobile x-ray system.

Electromedic Radiation

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing