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AQUALINER Hydrophilic Ni-Ti Alloy Guide Wire - Indonesia BPOM Medical Device Registration

AQUALINER Hydrophilic Ni-Ti Alloy Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501313787. The device is manufactured by NIPRO MEDICAL INDUSTRIES LTD, from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN WHEEL BEAM.

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
AQUALINER Hydrophilic Ni-Ti Alloy Guide Wire
Analysis ID: AKL 20501313787

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. MAIN WHEEL BEAM

AR Address

Perkantoran Duta Merlin Blok C No 58 jalan gajah mada

Registration Date

May 18, 2021

Expiry Date

Feb 04, 2026

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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