UBREATH™ PRO Spiro-meter System - Indonesia BPOM Medical Device Registration
UBREATH™ PRO Spiro-meter System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401917736. The device is manufactured by E-LINKCARE MEDITECH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GOLDEN MEDIKA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
E-LINKCARE MEDITECH CO., LTD.Country of Origin
China
Authorized Representative
GOLDEN MEDIKA MANDIRIAR Address
Jl. Raya Kalirungkut 27 Blok C-65
Registration Date
Sep 02, 2023
Expiry Date
Jun 07, 2028
Product Type
Diagnostic Anesthesia Equipment
Diagnostic spirometer.
Non Radiation Electromedics
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