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AGFA Mobile Digital Radiographic X-Ray System - DX-D 100 - Indonesia BPOM Medical Device Registration

AGFA Mobile Digital Radiographic X-Ray System - DX-D 100 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501812001. The device is manufactured by SEDECAL (SOCIEDAD ESPANOLA DE ELECTROMEDICINA Y CALIDAD, S.A.) from Spain, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GEVAERT AGFA HEALTHCARE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
AGFA Mobile Digital Radiographic X-Ray System - DX-D 100
Analysis ID: AKL 21501812001

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Spain

Authorized Representative

PT. GEVAERT AGFA HEALTHCARE INDONESIA

AR Address

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

Registration Date

Sep 21, 2023

Expiry Date

Dec 31, 2027

Product Type

Diagnostic Radiology Equipment

Mobile x-ray system.

Electromedic Radiation

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