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DEFIGARD HD-7 - Indonesia BPOM Medical Device Registration

DEFIGARD HD-7 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505123101. The device is manufactured by SCHILLER MEDICAL from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MULYA HUSADA JAYA.

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
DEFIGARD HD-7
Analysis ID: AKL 30505123101

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

SCHILLER MEDICAL

Country of Origin

France

Authorized Representative

MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO. 2-A

Registration Date

Nov 24, 2023

Expiry Date

Oct 31, 2025

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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