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GENKI EDGE Chest X-Ray Computer Aided Detection Software - Indonesia BPOM Medical Device Registration

GENKI EDGE Chest X-Ray Computer Aided Detection Software is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420605. The device is manufactured by DEEPTEK MEDICAL IMAGING PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRITRA PRIMA 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
GENKI EDGE Chest X-Ray Computer Aided Detection Software
Analysis ID: AKL 21501420605

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. TRITRA PRIMA INDONESIA

AR Address

Central Park Cikarang Blok A1 No. 02

Registration Date

Sep 10, 2024

Expiry Date

May 27, 2029

Product Type

Diagnostic Radiology Equipment

Chest X-Ray Computer Aided Detection

Non Radiation Electromedics

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