CARESTATION 620 A1 - Indonesia BPOM Medical Device Registration
CARESTATION 620 A1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403614553. The device is manufactured by DATEX-OHMEDA, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DATEX-OHMEDA, INC.Country of Origin
United States
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
Jul 12, 2023
Expiry Date
Apr 18, 2028
Product Type
Therapeutic Anesthesia Equipment
Gas machine for anesthesia or analgesia.
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