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BEXCORE Probe - Indonesia BPOM Medical Device Registration

BEXCORE Probe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801123040. The device is manufactured by MEDICAL PARK CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CUBE SUCCESS 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
BEXCORE Probe
Analysis ID: AKL 20801123040

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

CUBE SUCCESS INDONESIA

AR Address

SOHO PODOMORO CITY UNIT 38.16, JL. S. PARMAN KAV. 28

Registration Date

Jun 21, 2024

Expiry Date

Jun 17, 2029

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument

Non Electromedic Sterile

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