Pure Global

MEK Multi Parameter Patient Monitor - Indonesia BPOM Medical Device Registration

MEK Multi Parameter Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502310039. The device is manufactured by MEKICS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PERMANA PUTRA MANDIRI.

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
MEK Multi Parameter Patient Monitor
Analysis ID: AKL 20502310039

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEKICS CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. PERMANA PUTRA MANDIRI

AR Address

Taman Mini Pintu II Atas No.9 Jakarta Timur

Registration Date

Oct 07, 2019

Expiry Date

May 15, 2024

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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