TUOREN Tracheostomy Tube - Indonesia BPOM Medical Device Registration
TUOREN Tracheostomy Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403125450. The device is manufactured by HENAN TUOREN MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOMEDIKA SOLUSINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HENAN TUOREN MEDICAL DEVICE CO., LTD.Country of Origin
China
Authorized Representative
PT. INDOMEDIKA SOLUSINDOAR Address
Jalan Raya Bekasi Timur KM 17 No. 06 RT 016 RW 001
Registration Date
Jun 27, 2023
Expiry Date
Jun 01, 2025
Product Type
Therapeutic Anesthesia Equipment
Tracheostomy tube and tube cuff.
Non Electromedic Sterile
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