DAF - Anaesthetic Filter - Electrostatic - Indonesia BPOM Medical Device Registration
DAF - Anaesthetic Filter - Electrostatic is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403022643. The device is manufactured by FAIRMONT MEDICAL PRODUCTS PTY LTD from Australia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOSOPHA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FAIRMONT MEDICAL PRODUCTS PTY LTDCountry of Origin
Australia
Authorized Representative
INDOSOPHA SAKTIAR Address
JL. MAMPANG PRAPATAN RAYA NO.1
Registration Date
Aug 26, 2024
Expiry Date
Aug 05, 2026
Product Type
Therapeutic Anesthesia Equipment
Breathing circuit bacterial filter.
Non Electromedic Non Sterile
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