GEUDER XENOTRON III - Indonesia BPOM Medical Device Registration
GEUDER XENOTRON III is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201320418. The device is manufactured by GEUDER AG from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GEUDER AGCountry of Origin
Germany
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Nov 21, 2023
Expiry Date
Apr 06, 2026
Product Type
Diagnostic Eye Equipment
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