APC 2 (for VIO ) Argon Plasma Coagulation - Indonesia BPOM Medical Device Registration
APC 2 (for VIO ) Argon Plasma Coagulation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603515178. The device is manufactured by ERBE ELEKTROMEDIZIN GMBH. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ERBE ELEKTROMEDIZIN GMBH.Country of Origin
Germany
Authorized Representative
PT. SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Sep 07, 2023
Expiry Date
Dec 31, 2025
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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