Pure Global

VALISTA Non Compliant Balloon Dilatation Catheter - Indonesia BPOM Medical Device Registration

VALISTA Non Compliant Balloon Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505420077. The device is manufactured by DOLPHIN LIFE SCIENCE INDIA, LLP from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is INDOMED PHARMA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : D
VALISTA Non Compliant Balloon Dilatation Catheter
Analysis ID: AKL 30505420077

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

INDOMED PHARMA

AR Address

Kelapa Gading Hyper Mall, Lantai Dasar Blok B10 No. 03 (DB1003), Jakarta Utara

Registration Date

Jun 10, 2024

Expiry Date

Aug 10, 2028

Product Type

Therapeutic Cardiology Equipment

Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing