Pure Global

MOBILETT Elara Max - Indonesia BPOM Medical Device Registration

MOBILETT Elara Max is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220252. The device is manufactured by SOCIEDAD ESPANOLA DE ELECTROMEDICINA Y CALIDAD, S.A. (SEDECAL). from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SIEMENS HEALTHINEERS INDONESIA.

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
MOBILETT Elara Max
Analysis ID: AKL 21501220252

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Spain

Authorized Representative

PT. SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88

Registration Date

Dec 13, 2024

Expiry Date

Oct 14, 2029

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