Pure Global

TRIFECTA Valve with Glide Technology - Indonesia BPOM Medical Device Registration

TRIFECTA Valve with Glide Technology is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503022531. The device is manufactured by ST. JUDE MEDICAL COSTA RICA LTDA from Costa Rica, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TRANSMEDIC 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
TRIFECTA Valve with Glide Technology
Analysis ID: AKL 30503022531

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Costa Rica

Authorized Representative

PT. TRANSMEDIC INDONESIA

AR Address

PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137

Registration Date

Jul 08, 2020

Expiry Date

Dec 31, 2024

Product Type

Prosthetic Cardiology Equipment

Replacement heart valve.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing