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Venous Smartcanula - Indonesia BPOM Medical Device Registration

Venous Smartcanula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504420074. The device is manufactured by SMARTCANULA LLC from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULYA HUSADA JAYA.

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
Venous Smartcanula
Analysis ID: AKL 20504420074

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SMARTCANULA LLC

Country of Origin

Switzerland

Authorized Representative

PT. MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO. 2-A

Registration Date

Jun 20, 2024

Expiry Date

Nov 14, 2026

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass vascular catheter, cannula, or tubing.

Non Electromedic Sterile

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