RIZKIMED Endotracheal Tube Reinforced - Indonesia BPOM Medical Device Registration
RIZKIMED Endotracheal Tube Reinforced is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321749. The device is manufactured by NANCHANG KANGHUA HEALTH MATERIALS CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is RIZQULLAH MEDISKA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NANCHANG KANGHUA HEALTH MATERIALS CO., LTDCountry of Origin
China
Authorized Representative
RIZQULLAH MEDISKA INDONESIAAR Address
Perum Pabuaran Indah Blok i 6 No.2 Rt 012 Rw 017 Jalan Alpukat IV Pabuaran Cibinong
Registration Date
Nov 14, 2023
Expiry Date
Nov 13, 2026
Product Type
Therapeutic Anesthesia Equipment
Tracheal tube.
Non Electromedic Sterile

