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MAOR Infusion Pump i7 - Indonesia BPOM Medical Device Registration

MAOR Infusion Pump i7 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902127600. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
MAOR Infusion Pump i7
Analysis ID: AKL 20902127600

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ARTHA MEDIKA SENTOSA

AR Address

JL. GAGAK HITAM/RING ROAD NO. 1 A-B KEL. SEI SIKAMBING B KEC. MEDAN SUNGGAL

Registration Date

Dec 05, 2021

Expiry Date

Oct 08, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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