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EDAN Patient Monitor - Indonesia BPOM Medical Device Registration

EDAN Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502814616. The device is manufactured by EDAN INSTRUMENTS, INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NUSANTARA MEDCARE INTERNATIONAL.

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
EDAN Patient Monitor
Analysis ID: AKL 20502814616

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. NUSANTARA MEDCARE INTERNATIONAL

AR Address

Jl. Raya Prancis No.2 Pergd. Pantai Indah Dadap Blok HC/1. kel. Dadap. Kec. Kosambi. Kab Tangerang

Registration Date

Jul 01, 2022

Expiry Date

Feb 14, 2027

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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