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CAPIOX SX Hollow Fiber Oxygenator - Indonesia BPOM Medical Device Registration

CAPIOX SX Hollow Fiber Oxygenator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504304516. The device is manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TERUMO 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
CAPIOX SX Hollow Fiber Oxygenator
Analysis ID: AKL 20504304516

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. TERUMO INDONESIA

AR Address

Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta

Registration Date

May 28, 2020

Expiry Date

Apr 15, 2025

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass oxygenator.

Non Electromedic Sterile

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