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ADVA GLIDE - PTCA Balloon Catheter (Semi Compliant) - Indonesia BPOM Medical Device Registration

ADVA GLIDE - PTCA Balloon Catheter (Semi Compliant) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505124931. The device is manufactured by ADVANCED MEDTECH SOLUTIONS PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDICAL LYNAS.

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
ADVA GLIDE - PTCA Balloon Catheter (Semi Compliant)
Analysis ID: AKL 20505124931

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

MEDICAL LYNAS

AR Address

Ruko Cibubur Villa 5 No. 3, Jl. Raya Kranggan Km.1 Bekasi

Registration Date

Aug 10, 2021

Expiry Date

Aug 07, 2024

Product Type

Therapeutic Cardiology Equipment

Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Non Electromedic Sterile

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