GE Anesthesia Face Mask Silicone Reusable - Indonesia BPOM Medical Device Registration
GE Anesthesia Face Mask Silicone Reusable is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403021433. 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 GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FLEXICARE MEDICAL (DONGGUAN) LIMITEDCountry of Origin
China
Authorized Representative
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
Anesthetic gas mask.
Non Electromedic Non Sterile
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