GE Reusable Smoothbore Tube - Indonesia BPOM Medical Device Registration
GE Reusable Smoothbore Tube is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403021313. The device is manufactured by FLEXICARE MEDICAL (DONGGUAN) LIMITED from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FLEXICARE MEDICAL (DONGGUAN) LIMITEDCountry of Origin
China
Authorized Representative
PT. GE OPERATIONS INDONESIAAR Address
South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430
Registration Date
Mar 07, 2023
Expiry Date
Jan 16, 2028
Product Type
Therapeutic Anesthesia Equipment
Airway connector.
Non Electromedic Non Sterile
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