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AGFA Drystar AXYS Imager - Indonesia BPOM Medical Device Registration

AGFA Drystar AXYS Imager is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501910575. The device is manufactured by AGFA-GEVAERT HEALTHCARE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
AGFA Drystar AXYS Imager
Analysis ID: AKL 21501910575

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. GEVAERT-AGFA HEALTHCARE INDONESIA

AR Address

Jl Kesehatan Raya No 23C, Bintaro

Registration Date

Feb 08, 2019

Expiry Date

Dec 31, 2023

Product Type

Diagnostic Radiology Equipment

Medical image hardcopy device.

Non Radiation Electromedics

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