TURBINATOR™ Wall - Indonesia BPOM Medical Device Registration
TURBINATOR™ Wall is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603717553. The device is manufactured by ARTHROCARE CORPORATION S.R.L. from Costa Rica, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.
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TURBINATOR™ Wand
Risk Classification
Product Class
Kelas : 2
Manufacturer
ARTHROCARE CORPORATION S.R.L.Country of Origin
Costa Rica
Authorized Representative
PT. TAWADA HEALTHCAREAR Address
Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5
Registration Date
Jan 21, 2022
Expiry Date
Dec 31, 2024
Product Type
Surgical Equipment
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