Pure Global

SHUNMEI Balloon Inflation Devices - Indonesia BPOM Medical Device Registration

SHUNMEI Balloon Inflation Devices is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320896. The device is manufactured by SHUNMEI MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. AMITHYA SATYA LARAS.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
SHUNMEI Balloon Inflation Devices
Analysis ID: AKL 20501320896

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. AMITHYA SATYA LARAS

AR Address

Gedung Ganeca, Jl. Raya Pasar Minggu No. 234A, Duren Tiga, Pancoran, Jakarta Selatan 12760

Registration Date

Jul 17, 2023

Expiry Date

Feb 20, 2026

Product Type

Diagnostic Cardiology Equipment

Angiographic Injector and Syringe

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name