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MDF 787 XP Deluxe Infant & Neonatal Stethoscope - Indonesia BPOM Medical Device Registration

MDF 787 XP Deluxe Infant & Neonatal Stethoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10501806212. The device is manufactured by MDF INSTRUMENTS MEDIFRIEND, INC. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FA ANTARES MEDIKA.

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 : A
MDF 787 XP Deluxe Infant & Neonatal Stethoscope
Analysis ID: AKL 10501806212

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

Ruko Golden Boulevard Blok i No 7 BSD City

Registration Date

Mar 13, 2022

Expiry Date

Dec 28, 2026

Product Type

Diagnostic Cardiology Equipment

Stethoscope.

Non Electromedic Non Sterile

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