SYAS RESPIRA Flexi with Accessories - Indonesia BPOM Medical Device Registration
SYAS RESPIRA Flexi with Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420810. The device is manufactured by BEIJING AEONMED CO., LTD., from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KURNIA SELARAS SEJAHTERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING AEONMED CO., LTD.,Country of Origin
China
Authorized Representative
PT. KURNIA SELARAS SEJAHTERAAR Address
Foresta Business Loft 2 Unit 32-33 Jl. BSD Raya Utama
Registration Date
Dec 10, 2024
Expiry Date
Dec 09, 2027
Product Type
Therapeutic Anesthesia Equipment
External negative pressure ventilator.
Non Radiation Electromedics
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