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AGFA ORTHO CP-GU M Medical X-Ray Film - Indonesia BPOM Medical Device Registration

AGFA ORTHO CP-GU M Medical X-Ray Film is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11501816613. The device is manufactured by AGFA N.V. from Belgium, and is classified as Risk Class Kelas Resiko : A. 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 : A
AGFA ORTHO CP-GU M Medical X-Ray Film
Analysis ID: AKL 11501816613

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

AGFA N.V.

Country of Origin

Belgium

Authorized Representative

GEVAERT AGFA HEALTHCARE INDONESIA

AR Address

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

Registration Date

Oct 09, 2023

Expiry Date

Apr 05, 2027

Product Type

Diagnostic Radiology Equipment

Radiographic film.

Non Electromedic Non Sterile

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