GEUDER Endotron 532 nm Surgical System - Indonesia BPOM Medical Device Registration
GEUDER Endotron 532 nm Surgical System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203320385. The device is manufactured by GEUDER AG 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
GEUDER AGCountry 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 14, 2023
Expiry Date
Apr 06, 2026
Product Type
Surgical Eye Equipment
Ophthalmic photocoagulator.
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