EVA NEXUS ™, Phaco emulsification system - Indonesia BPOM Medical Device Registration
EVA NEXUS ™, Phaco emulsification system is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203220002. The device is manufactured by D.O.R.C. DUTCH OPHTHALMIC RESEARCH CENTER (INTERNATIONAL) B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PERFECT SINGLE OPTICS.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Netherlands
Authorized Representative
PERFECT SINGLE OPTICSAR Address
Jl. Pintu Air Raya No. 36 KL. Pasar baru
Registration Date
Feb 02, 2023
Expiry Date
Dec 31, 2026
Product Type
Surgical Eye Equipment
Phacofragmentation system.
Non Radiation Electromedics
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