Pure Global

EPIbeam - Indonesia BPOM Medical Device Registration

EPIbeam is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220431. The device is manufactured by DOSISOFT SA from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ELEKTA MEDICAL SOLUTIONS.

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 : B
EPIbeam
Analysis ID: AKL 21501220431

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DOSISOFT SA

Country of Origin

France

Authorized Representative

ELEKTA MEDICAL SOLUTIONS

AR Address

Cowell Tower Lt. 7 Unit 02A, Jl. Senen Raya No. 135

Registration Date

Sep 10, 2022

Expiry Date

Apr 27, 2027

Product Type

Diagnostic Radiology Equipment

(Dihapus) Picture archiving and communications system.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from DOSISOFT SA
Products from the same manufacturer (1 products)