Pure Global

PACEL Bipolar Pacing Catheter- Flow Directed - Indonesia BPOM Medical Device Registration

PACEL Bipolar Pacing Catheter- Flow Directed is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504814283. The device is manufactured by ST JUDE MEDICAL from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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
PACEL Bipolar Pacing Catheter- Flow Directed
Analysis ID: AKL 20504814283

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ST JUDE MEDICAL

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5

Registration Date

Oct 13, 2020

Expiry Date

Aug 13, 2025

Product Type

Prosthetic Cardiology Equipment

Cardiovascular temporary pacemaker electrode.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from ST JUDE MEDICAL
Products from the same manufacturer (2 products)