INTERSURGICAL Humidification Chamber - Indonesia BPOM Medical Device Registration
INTERSURGICAL Humidification Chamber is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403716102. The device is manufactured by INTERSURGICAL LIMITED. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MADESA SEJAHTERA UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INTERSURGICAL LIMITED.Country of Origin
United Kingdom
Authorized Representative
PT. MADESA SEJAHTERA UTAMAAR Address
JL. GUNUNG SAHARI RAYA 51-A NO.14, GUNUNG SAHARI SELATAN
Registration Date
Mar 07, 2024
Expiry Date
Sep 14, 2026
Product Type
Therapeutic Anesthesia Equipment
Respiratory gas humidifier.
Non Electromedic Non Sterile
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