Pure Global

MEDTRONIC Percutaneous Lead Introducer - Indonesia BPOM Medical Device Registration

MEDTRONIC Percutaneous Lead Introducer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501124282. The device is manufactured by GREATBATCH MEDICAL, S. DE R.L. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. 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 : B
MEDTRONIC Percutaneous Lead Introducer
Analysis ID: AKL 20501124282

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

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

Registration Date

Jul 28, 2021

Expiry Date

Jan 13, 2026

Product Type

Diagnostic Cardiology Equipment

Catheter introducer

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
Other Products from GREATBATCH MEDICAL, S. DE R.L. DE C.V.
Products from the same manufacturer (2 products)