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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.

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Risk Class Kelas Resiko : C
EyRIS SELENA+
Analysis ID: AKL 21201120164

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

EYRIS PTE LTD

Country of Origin

Singapore

Authorized Representative

PT. TRITRA PRIMA INDONESIA

AR 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

Non Radiation Electromedics

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