PIGEON INFANT RESUSCITATION - Indonesia BPOM Medical Device Registration
PIGEON INFANT RESUSCITATION is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220655. The device is manufactured by GUANGDONG PIGEON MEDICAL APPARATUS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MANDIRI JAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGDONG PIGEON MEDICAL APPARATUS CO., LTD.Country of Origin
China
Authorized Representative
PT. MANDIRI JAYA MEDIKAAR Address
Graha Mas Fatmawati Blok B No. 20, Jl. RS. Fatmawati No. 71
Registration Date
Sep 06, 2022
Expiry Date
Jun 17, 2027
Product Type
Therapeutic Anesthesia Equipment
Manual emergency ventilator.
Non Electromedic Non Sterile
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