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AGFA CR 12-X DIGITIZER - Indonesia BPOM Medical Device Registration

AGFA CR 12-X DIGITIZER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501220327. The device is manufactured by AGFA (WUXI) IMAGING CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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 CR 12-X DIGITIZER
Analysis ID: AKL 21501220327

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

GEVAERT AGFA HEALTHCARE INDONESIA

AR Address

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

Registration Date

Nov 17, 2023

Expiry Date

Dec 31, 2027

Product Type

Diagnostic Radiology Equipment

Medical image digitizer.

Non Radiation Electromedics

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