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RIZKIMED Foley Catheter - Indonesia BPOM Medical Device Registration

RIZKIMED Foley Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320870. The device is manufactured by NANCHANG KANGHUA HEALTH MATERIALS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RIZQULLAH MEDISKA 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
RIZKIMED Foley Catheter
Analysis ID: AKL 20805320870

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. RIZQULLAH MEDISKA INDONESIA

AR Address

Perum Pabuaran Indah Blok i 6 No.2 Rt 012 Rw 017 Jalan Alpukat IV Pabuaran Cibinong

Registration Date

Aug 24, 2023

Expiry Date

Aug 23, 2026

Product Type

Therapeutic Gastroenterology-Urology Equipment

Urological catheter and accessories.

Non Electromedic Sterile

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