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ABADA Latex Foley Catheter Three-Way - Indonesia BPOM Medical Device Registration

ABADA Latex Foley Catheter Three-Way is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220048. The device is manufactured by HENSO MEDICAL (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MUZAMAL VENTURES 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
ABADA Latex Foley Catheter Three-Way
Analysis ID: AKL 20805220048

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MUZAMAL VENTURES INDONESIA

AR Address

JL. PANCASILA V NO. 66 A

Registration Date

Feb 25, 2022

Expiry Date

Feb 24, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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