Pure Global

NITI - S Enteral Colonic Covered Stent - Indonesia BPOM Medical Device Registration

NITI - S Enteral Colonic Covered Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805026529. The device is manufactured by TAEWOONG MEDICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDISON JAYA RAYA.

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 : C
NITI - S Enteral Colonic Covered Stent
Analysis ID: AKL 20805026529

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. MEDISON JAYA RAYA

AR Address

JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN

Registration Date

Dec 29, 2021

Expiry Date

Aug 03, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Biliary catheter and accessories.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing