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MEDG All Silicone Foley Catheter 3way - Indonesia BPOM Medical Device Registration

MEDG All Silicone Foley Catheter 3way is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320975. The device is manufactured by JIANGSU PROVINCE HUAXING MEDICAL APPARATUS INDUSTRY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALEXA MEDIKA.

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
MEDG All Silicone Foley Catheter 3way
Analysis ID: AKL 20805320975

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ALEXA MEDIKA

AR Address

Jl. Yos Sudarso Komplek Graha Niaga Blok C No. 14

Registration Date

Oct 22, 2023

Expiry Date

Mar 10, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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