Suprasorb Liquacel Ag - Indonesia BPOM Medical Device Registration
Suprasorb Liquacel Ag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603323232. The device is manufactured by SPECIALITY FIBRES AND MATERIAIS LTD from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NUSA ASIA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SPECIALITY FIBRES AND MATERIAIS LTDCountry of Origin
United States
Authorized Representative
PT. NUSA ASIA MEDIKAAR Address
Rukan CBD, Green Lake City F No. 15 Ketapang. Cipondoh
Registration Date
Feb 13, 2023
Expiry Date
May 31, 2027
Product Type
Surgical Equipment
Hydrophilic wound dressing
Non Electromedic Sterile
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