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AXI CATH Female Catheter - Indonesia BPOM Medical Device Registration

AXI CATH Female Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805813228. The device is manufactured by JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BIO AXION HEALTHINDO.

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
AXI CATH Female Catheter
Analysis ID: AKL 20805813228

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BIO AXION HEALTHINDO

AR Address

Komplek Golden Plaza Blok G39 - G42 Jl. RS Fatmawati No. 15

Registration Date

Mar 25, 2021

Expiry Date

Dec 19, 2023

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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