Pure Global

SMAM Mobile C-Arm - Indonesia BPOM Medical Device Registration

SMAM Mobile C-Arm is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501915466. The device is manufactured by SMAM S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SATYA ABADI VISIMED.

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
SMAM Mobile C-Arm
Analysis ID: AKL 21501915466

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SMAM S.R.L.

Country of Origin

Italy

Authorized Representative

PT. SATYA ABADI VISIMED

AR Address

Ruko Sentra Menteng Blok MN-28 Bintaro Jaya Sektor 7 Pondok Jaya Pondok Aren Tangerang 15224

Registration Date

Mar 01, 2023

Expiry Date

Jul 13, 2027

Product Type

Diagnostic Radiology Equipment

Image-intensified fluoroscopic x-ray system.

Electromedic Radiation

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing