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NITI - S Biliary Stent - Indonesia BPOM Medical Device Registration

NITI - S Biliary Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420544. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
NITI - S Biliary Stent
Analysis ID: AKL 20805420544

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

Oct 25, 2024

Expiry Date

Aug 03, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Biliary catheter and accessories.

Non Electromedic Sterile

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