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ZIPwire Hydrophilic Guidewire - Indonesia BPOM Medical Device Registration

ZIPwire Hydrophilic Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320843. The device is manufactured by VENUSA DE MEXICO DE S.RL DE C.V from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is BOSTON SCIENTIFIC INDONESIA.

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
ZIPwire Hydrophilic Guidewire
Analysis ID: AKL 20805320843

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

BOSTON SCIENTIFIC INDONESIA

AR Address

Prudential Tower lantai 28 Jl. Jend. Sudirman Kav. 79

Registration Date

Jul 27, 2023

Expiry Date

Apr 07, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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