SURGAID Single Use Sterile Minimally Invasive Fascia Closure Device - Indonesia BPOM Medical Device Registration
SURGAID Single Use Sterile Minimally Invasive Fascia Closure Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421514. The device is manufactured by SURGAID MEDICAL (XIAMEN) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOMAKMUR DWI LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SURGAID MEDICAL (XIAMEN) CO., LTD.Country of Origin
China
Authorized Representative
PT. INDOMAKMUR DWI LESTARIAR Address
Ruko Mutiara taman palem blok A18 no 17 RT.7/RW.14, Cengkareng Tim., Kecamatan Cengkareng, Kota Jakarta Barat, Daerah Khusus Ibukota Jakarta 11730
Registration Date
Jul 11, 2024
Expiry Date
Jun 26, 2026
Product Type
Surgical Equipment
Implantable staple.
Non Electromedic Sterile
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