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MEDITEC ENGLAND Patient Monitor - Indonesia BPOM Medical Device Registration

MEDITEC ENGLAND Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502511565. The device is manufactured by MEDITEC INTERNATIONAL ENGLAND LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTIGUNA CIPTASENTOSA.

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
MEDITEC ENGLAND Patient Monitor
Analysis ID: AKL 20502511565

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. MULTIGUNA CIPTASENTOSA

AR Address

Surapati Core Blok M No.1 Jl. Phh. Mustofa No. 39 Bandung 022-87241400

Registration Date

Jul 15, 2022

Expiry Date

Jun 30, 2024

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Radiation Electromedics

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