EyRIS SELENA+ - Indonesia BPOM Medical Device Registration
EyRIS SELENA+ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201120164. The device is manufactured by EYRIS PTE LTD from Singapore, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRITRA PRIMA INDONESIA.
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
Manufacturer
EYRIS PTE LTDCountry of Origin
Singapore
Authorized Representative
PT. TRITRA PRIMA INDONESIAAR Address
Taman Sari Persada Blok F-1 Nomor 10
Registration Date
Jan 10, 2021
Expiry Date
Oct 26, 2025
Product Type
Diagnostic Eye Equipment
Retinal Diagnostic Software Device
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