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ILOODA Ultra Beaujet - Indonesia BPOM Medical Device Registration

ILOODA Ultra Beaujet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902914594. The device is manufactured by ILOODA CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ZHENGAN INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
ILOODA Ultra Beaujet
Analysis ID: AKL 20902914594

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ILOODA CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. ZHENGAN INDONESIA

AR Address

Ruko Duren Sawit Center No. 8E, Jl. Raya Duren Sawit, Kel. Klender, Kec. Duren Sawit, Jakarta Timur

Registration Date

Jul 29, 2019

Expiry Date

Mar 18, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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