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DIMED Infusion Pump - Indonesia BPOM Medical Device Registration

DIMED Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902124337. The device is manufactured by SHENZHEN HAWK MEDICAL INSTRUMENT CO,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SUMBER MAKMUR BERDIKARI.

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
DIMED Infusion Pump
Analysis ID: AKL 20902124337

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SUMBER MAKMUR BERDIKARI

AR Address

RUKAN CROWN GREEN LAKE CITY BLOK B NO. 8, PETIR, TANGERANG 15147

Registration Date

Jul 20, 2021

Expiry Date

Jul 19, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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DJ Fang

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