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MEDUCORE Standard - Indonesia BPOM Medical Device Registration

MEDUCORE Standard is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505220072. The device is manufactured by WEINMANN EMERGENCY MEDICAL TECHNOLOGY GMBH + CO. KG from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ALFA MEDIKA INDONESIA.

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 : D
MEDUCORE Standard
Analysis ID: AKL 30505220072

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Germany

Authorized Representative

PT. ALFA MEDIKA INDONESIA

AR Address

RUKO BOULEVARD TEKNO BLOK AA NO. 11, RT011/001, JL. TEKNO WIDYA

Registration Date

Apr 22, 2024

Expiry Date

Mar 31, 2026

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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