RENASYS F Foam Dressing Kit with Softport - Indonesia BPOM Medical Device Registration
RENASYS F Foam Dressing Kit with Softport is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603022688. The device is manufactured by VIANT MEDICAL LLC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ENSEVAL PUTERA MEGATRADING TBK.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIANT MEDICAL LLCCountry of Origin
United States
Authorized Representative
PT. ENSEVAL PUTERA MEGATRADING TBKAR Address
Jalan Pulo Lentut No.10 Kawasan Industri Pulogadung, Jakarta Timur
Registration Date
Sep 18, 2023
Expiry Date
Dec 31, 2025
Product Type
Surgical Equipment
Powered suction pump.
Non Electromedic Sterile
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