Pure Global

WALLFLEX Esophageal Partially Covered Stent System - Indonesia BPOM Medical Device Registration

WALLFLEX Esophageal Partially Covered Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21602512382. The device is manufactured by BOSTON SCIENTIFIC LIMITED from Ireland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BOSTON SCIENTIFIC 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
WALLFLEX Esophageal Partially Covered Stent System
Analysis ID: AKL 21602512382

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Ireland

Authorized Representative

PT. BOSTON SCIENTIFIC INDONESIA

AR Address

PRUDENTIAL TOWER, LT. 28, JL. JEND. SUDIRMAN KAV. 79

Registration Date

Jan 30, 2025

Expiry Date

Apr 20, 2027

Product Type

Prosthetic Surgical Equipment

Esophageal prosthesis.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing