DURAFIBER AT - Indonesia BPOM Medical Device Registration
DURAFIBER AT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603912401. The device is manufactured by SMITH & NEPHEW MEDICAL LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ENSEVAL PUTERA MEGATRADING TBK.
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DURAFIBER AG
Risk Classification
Product Class
Kelas : 1
Manufacturer
SMITH & NEPHEW MEDICAL LTD.Country of Origin
United Kingdom
Authorized Representative
PT. ENSEVAL PUTERA MEGATRADING TBKAR Address
Jalan Pulo Lentut No.10 Kawasan Industri Pulogadung, Jakarta Timur
Registration Date
Sep 24, 2023
Expiry Date
Dec 31, 2025
Product Type
Surgical Equipment
Occlusive wound dressing.
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