Pure Global

AGFA Digital Radiographic X-ray System DR 400 - Indonesia BPOM Medical Device Registration

AGFA Digital Radiographic X-ray System DR 400 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501913541. The device is manufactured by AGFA-GEVAERT HEALTHCARE GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GEVAERT AGFA HEALTHCARE 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
AGFA Digital Radiographic X-ray System DR 400
Analysis ID: AKL 21501913541

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. GEVAERT AGFA HEALTHCARE INDONESIA

AR Address

Jl. Kesehatan Raya No. 23 C RT 010 RW 011

Registration Date

Oct 14, 2023

Expiry Date

Apr 05, 2027

Product Type

Diagnostic Radiology Equipment

Stationary x-ray system.

Electromedic Radiation

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from AGFA-GEVAERT HEALTHCARE GMBH
Products from the same manufacturer (1 products)