Pure Global

VENASEAL Closure System - Indonesia BPOM Medical Device Registration

VENASEAL Closure System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30504220035. The device is manufactured by MEDTRONIC IRELAND from Ireland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDTRONIC 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 : D
VENASEAL Closure System
Analysis ID: AKL 30504220035

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MEDTRONIC IRELAND

Country of Origin

Ireland

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Apr 27, 2022

Expiry Date

Feb 16, 2027

Product Type

Surgical Cardiology Equipment

Vascular closure device

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name