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3Flow Aspiration Catheter - Indonesia BPOM Medical Device Registration

3Flow Aspiration Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420039. The device is manufactured by ARTHESYS from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DCH AURIGA INDONESIA.

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 : C
3Flow Aspiration Catheter
Analysis ID: AKL 20501420039

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ARTHESYS

Country of Origin

France

Authorized Representative

PT. DCH AURIGA INDONESIA

AR Address

DCH AURIGA INDONESIA

Registration Date

Jan 20, 2024

Expiry Date

Jul 05, 2028

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

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