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ROSSMAX Stethoscope - Indonesia BPOM Medical Device Registration

ROSSMAX Stethoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10401713799. The device is manufactured by ROSSMAX (SHANGHAI) INCORPORATION LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDISINDO BAHANA.

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
ROSSMAX Stethoscope
Analysis ID: AKL 10401713799

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MEDISINDO BAHANA

AR Address

Rukan Graha Cempaka Mas Blok E No.15 Lt.3, Jl. Letjen Suprapto No.1, Jakarta Pusat

Registration Date

Apr 05, 2021

Expiry Date

Feb 21, 2025

Product Type

Diagnostic Anesthesia Equipment

Stethoscope head.

Non Electromedic Non Sterile

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