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PRONTO® V3 Extraction Catheter - Indonesia BPOM Medical Device Registration

PRONTO® V3 Extraction Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505911243. The device is manufactured by VASCULAR SOLUTIONS LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REKAMILENIUMINDO SELARAS.

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
PRONTO® V3 Extraction Catheter
Analysis ID: AKL 20505911243

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. REKAMILENIUMINDO SELARAS

AR Address

Jl. Tomang Raya No. 51B RT 01 RW 05

Registration Date

Nov 17, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic Cardiology Equipment

Embolectomy catheter.

Non Electromedic Sterile

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