MEDIGLOBE Medi Filift Tissue Reconstructive Material, Synthetic, Polymer, Absorbable - Indonesia BPOM Medical Device Registration
MEDIGLOBE Medi Filift Tissue Reconstructive Material, Synthetic, Polymer, Absorbable is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603221298. The device is manufactured by JINOH MECHADICAL CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PHARMINDO RHIZOME STURDY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JINOH MECHADICAL CO., LTD.Country of Origin
Korea
Authorized Representative
PT. PHARMINDO RHIZOME STURDYAR Address
Jalan Arowana No 98 Kel. Kebonagung Kec. Kaliwates
Registration Date
May 28, 2022
Expiry Date
Oct 16, 2024
Product Type
Surgical Equipment
Absorbable polydioxanone surgical suture.
Non Electromedic Sterile
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