DELVI CARE Nasal Oxygen Cannula - Indonesia BPOM Medical Device Registration
DELVI CARE Nasal Oxygen Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403321134. The device is manufactured by NINGBO MFLAB MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DELVI PRIMATAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
NINGBO MFLAB MEDICAL INSTRUMENTS CO., LTD.Country of Origin
China
Authorized Representative
PT. DELVI PRIMATAMAAR Address
Perum Mutiara Gading Timur Blok A8 No. 7-8 RT 001 RW 031 Kelurahan Mustika Jaya, Kecamatan Mustika Jaya - Kota Bekasi
Registration Date
Mar 14, 2023
Expiry Date
Mar 13, 2026
Product Type
Therapeutic Anesthesia Equipment
Nasal oxygen cannula.
Non Electromedic Non Sterile
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