WOWART MONO - Indonesia BPOM Medical Device Registration
WOWART MONO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421671. The device is manufactured by DERMALINE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MITRA HARAPAN MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DERMALINE CO., LTD.Country of Origin
Korea
Authorized Representative
PT. MITRA HARAPAN MANDIRIAR Address
The Bellezza Shopping Arcade Lt. 2 SA 69, 70 & 71, Jl. Letjen Soepeno No. 34 Arteri Permata Hijau
Registration Date
Jul 30, 2024
Expiry Date
May 26, 2029
Product Type
Surgical Equipment
Absorbable polydioxanone surgical suture.
Non Electromedic Sterile
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