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DAIWHA Infusion Pump - Indonesia BPOM Medical Device Registration

DAIWHA Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902914768. The device is manufactured by DAIWHA CORP. LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL MEDICAL PRESS.

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BPOM Registered
Risk Class Kelas Resiko : B
DAIWHA Infusion Pump
Analysis ID: AKL 20902914768

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DAIWHA CORP. LTD

Country of Origin

Korea

Authorized Representative

PT. GLOBAL MEDICAL PRESS

AR Address

Kompl.Green Garden AA-1/17 Jl.MH Thamrin KM 7 RT 04/RW 02 Kel.Panunggangan Utara Kec.Pinang.Kota Tangerang

Registration Date

Jul 29, 2019

Expiry Date

Mar 05, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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