Pure Global

MAOR Healfusion Infusion Pump - Indonesia BPOM Medical Device Registration

MAOR Healfusion Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902421469. The device is manufactured by HEDY MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ARTHA MEDIKA SENTOSA.

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 : B
MAOR Healfusion Infusion Pump
Analysis ID: AKL 20902421469

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ARTHA MEDIKA SENTOSA

AR Address

Ruko Rose Garden 8 No 21, Grand Galaxy City

Registration Date

Dec 16, 2024

Expiry Date

Nov 11, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from HEDY MEDICAL DEVICE CO., LTD.
Products from the same manufacturer (3 products)