TUOREN Guedel Airway - Indonesia BPOM Medical Device Registration
TUOREN Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403122236. The device is manufactured by HENAN TUOREN MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SINAR PANCA MEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HENAN TUOREN MEDICAL DEVICE CO., LTD.Country of Origin
China
Authorized Representative
SINAR PANCA MEDIKAAR Address
Ruko Sedayu Square Blok G-01/G-02, Jl. Lingkar Luar Barat, Kel. Cengkareng Barat, Kec. Cengkareng, Kota Adm. Jakarta Barat, Provinsi DKI Jakarta, Kode Pos 11730
Registration Date
Jul 10, 2023
Expiry Date
Mar 23, 2026
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway
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