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MAMBA Sirolimus Eluting PTCA Balloon Catheter - Indonesia BPOM Medical Device Registration

MAMBA Sirolimus Eluting PTCA Balloon Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505320221. The device is manufactured by FRISCH MEDICAL DEVICES PVT. LTD. from India, 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
MAMBA Sirolimus Eluting PTCA Balloon Catheter
Analysis ID: AKL 30505320221

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

MAIN REVASS MEDIKA

AR Address

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

Registration Date

Jun 02, 2023

Expiry Date

Jan 27, 2028

Product Type

Therapeutic Cardiology Equipment

Drug Eluting Balloon

Non Electromedic Sterile

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