Pure Global

RIZKIMED Disposable Infusion Set - Indonesia BPOM Medical Device Registration

RIZKIMED Disposable Infusion Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420259. The device is manufactured by LIAONING KANGYI MEDICAL EQUIPMENT 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
RIZKIMED Disposable Infusion Set
Analysis ID: AKL 20902420259

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

Mar 06, 2024

Expiry Date

Feb 06, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing