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SAPPHIRE Neuro Balloon Dilatation Catheter - Indonesia BPOM Medical Device Registration

SAPPHIRE Neuro Balloon Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003420061. The device is manufactured by ORBUSNEICH MEDICAL (SHENZHEN) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MAIN REVASS 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 : D
SAPPHIRE Neuro Balloon Dilatation Catheter
Analysis ID: AKL 31003420061

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

MAIN REVASS MEDIKA

AR Address

Jl. Dewi Sartika No. 4B RT 004/007 Kel. Cililitan Kec. Kramat jati

Registration Date

Jul 04, 2024

Expiry Date

Dec 15, 2028

Product Type

Therapeutic Neurology Equipment

Percutaneous catheter for neurovascular

Non Electromedic Sterile

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