PULMODYNE HME Filters - Indonesia BPOM Medical Device Registration
PULMODYNE HME Filters is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403220845. The device is manufactured by ENGINEERED MEDICAL SYSTEM MALAYSIAN SDN BHD from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAVINDRA PUTRAPRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ENGINEERED MEDICAL SYSTEM MALAYSIAN SDN BHDCountry of Origin
Malaysia
Authorized Representative
PT. RAVINDRA PUTRAPRATAMAAR Address
Pusat Niaga Duta Mas Fatmawati Blok B2-18. Jl. Fatmawati 39 - Cipete Utara Jakarta 12150
Registration Date
Nov 18, 2022
Expiry Date
Jul 29, 2024
Product Type
Therapeutic Anesthesia Equipment
Breathing circuit bacterial filter.
Non Electromedic Non Sterile
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