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Vivo ISAR - Indonesia BPOM Medical Device Registration

Vivo ISAR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503220083. The device is manufactured by TRANSLUMINA THERAPEUTICS LLP from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is ARQON MEDICAL SOLUTIONS.

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
Vivo ISAR
Analysis ID: AKL 30503220083

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

ARQON MEDICAL SOLUTIONS

AR Address

Rukan Niaga Gunung Sahari Blok B2 Jl Gunung Sahari Raya No 7

Registration Date

Aug 18, 2022

Expiry Date

Mar 31, 2027

Product Type

Prosthetic Cardiology Equipment

Drug eluting stent

Non Electromedic Sterile

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