Pure Global

HOKIDAI Video Flexible Endoscopy System - Indonesia BPOM Medical Device Registration

HOKIDAI Video Flexible Endoscopy System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801220398. The device is manufactured by HUGER MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KARUNIAJAYA ANDALAN PRIMA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
HOKIDAI Video Flexible Endoscopy System
Analysis ID: AKL 20801220398

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. KARUNIAJAYA ANDALAN PRIMA

AR Address

RUKO JALUR SUTERA TIMUR BLOK. 6B NO. 23 ALAM SUTERA, SERPONG, TANGERANG 15144.

Registration Date

Oct 21, 2022

Expiry Date

Jul 05, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing