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EDGE Endoscopic Instrument Control System - Indonesia BPOM Medical Device Registration

EDGE Endoscopic Instrument Control System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801420301. The device is manufactured by SHENZHEN EDGE MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PURE SOUTHEAST ASIA 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
EDGE Endoscopic Instrument Control System
Analysis ID: AKL 20801420301

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PURE SOUTHEAST ASIA INDONESIA

AR Address

Equity Tower, 26th Floor H, Kav 52-53, Jl. Jenderal Sudirman

Registration Date

Aug 09, 2024

Expiry Date

May 01, 2029

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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