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.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
ILOODA CO., LTD.Country of Origin
Korea
Authorized Representative
PT. ZHENGAN INDONESIAAR 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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YOUR LINE P(LA/CL) Suture with Needle
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SECRET DUO
ILOODA CO., LTD.
FRAXIS DUO
ILOODA CO., LTD.
FRAXIS
ILOODA CO., LTD.
SECRET
ILOODA CO., LTD.
CURES
ILOODA CO., LTD.
VIKINI
ILOODA CO., LTD.
EPILIA RF
ILOODA CO., LTD.

