CREATE BIOTECH Guedel Airway - Indonesia BPOM Medical Device Registration
CREATE BIOTECH Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403220946. The device is manufactured by CREATE BIOTECH CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEDMAX GLOBAL INDOTAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CREATE BIOTECH CO., LTD.Country of Origin
Taiwan (China)
Authorized Representative
MEDMAX GLOBAL INDOTAMAAR Address
Perum Taman Candiloka C3-7 Ngampelsari Candi Sidoarjo
Registration Date
Dec 12, 2022
Expiry Date
Oct 13, 2024
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway
Non Electromedic Non Sterile
