PIGEON Manual Breast Pump - Indonesia BPOM Medical Device Registration
PIGEON Manual Breast Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11104412747. The device is manufactured by PIGEON CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULTI INDOCITRA. TBK.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
PIGEON CORPORATIONCountry of Origin
Japan
Authorized Representative
PT. MULTI INDOCITRA. TBKAR Address
Green Central City, Commercial Area Lantai 6 Jl Gajah Mada No.188, Jakarta 11120
Registration Date
Apr 28, 2022
Expiry Date
Sep 20, 2026
Product Type
Therapeutic Obstetric and Gynecological Equipment
Nonpowered breast pump.
Non Electromedic Non Sterile
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