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ARES Ballon Inflantion Device - Indonesia BPOM Medical Device Registration

ARES Ballon Inflantion Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501124397. The device is manufactured by ARES MEDIKAL SANAYI TICARET LIMITED SIKERTI from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BISAWI GROWS IN HARMONY.

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 : B
ARES Ballon Inflantion Device
Analysis ID: AKL 20501124397

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. BISAWI GROWS IN HARMONY

AR Address

Graha Kencana Blok EU Jl. Raya Perjuangan No.88 Kebun Jeruk Jakarta Barat

Registration Date

Jul 22, 2021

Expiry Date

Dec 31, 2025

Product Type

Diagnostic Cardiology Equipment

Angiographic Injector and Syringe

Non Electromedic Sterile

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