Pure Global

SKINTACT ECG Electrode - Indonesia BPOM Medical Device Registration

SKINTACT ECG Electrode is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502311394. The device is manufactured by LEONHARD LANG GMBH. from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL MEDIKA PRIMA.

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
SKINTACT ECG Electrode
Analysis ID: AKL 20502311394

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Austria

Authorized Representative

PT. ENSEVAL MEDIKA PRIMA

AR Address

JL. PULO LENTUT NO.12, LT.1 UNIT 1C & LT.2 UNIT 2A, KAWASAN INDUSTRI PULOGADUNG

Registration Date

Feb 13, 2022

Expiry Date

Mar 31, 2025

Product Type

Monitoring Cardiology Equipment

Electrocardiograph electrode.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing