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EAGLECARE EM-M80 Patient Monitor - Indonesia BPOM Medical Device Registration

EAGLECARE EM-M80 Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502911874. The device is manufactured by NORTHEN MEDITEC LIMITED from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INAHO JAYA LESTARI.

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.

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BPOM Registered
Risk Class Kelas Resiko : B
EAGLECARE EM-M80 Patient Monitor
Analysis ID: AKL 20502911874

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INAHO JAYA LESTARI

AR Address

Jl. Tentara Pelajar No. 42 - 42A

Registration Date

Mar 25, 2022

Expiry Date

Mar 25, 2025

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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