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AUROFLEX EV Aspheric Hydrophilic Foldable Intraocular Lens - Indonesia BPOM Medical Device Registration

AUROFLEX EV Aspheric Hydrophilic Foldable Intraocular Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202714141. The device is manufactured by AUROLAB from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MAIN INDEPENDENT MEDEQ.

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BPOM Registered
Risk Class Kelas Resiko : D
AUROFLEX EV Aspheric Hydrophilic Foldable Intraocular Lens
Analysis ID: AKL 31202714141

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

AUROLAB

Country of Origin

India

Authorized Representative

PT. MAIN INDEPENDENT MEDEQ

AR Address

Ruko Graha Mas Pemuda Blok AC-19 jL. Pemuda Blok AC-19 Jl. Pemuda Kel. Jati Kec. Pulo Gadung Jakarta Timur

Registration Date

Jun 30, 2022

Expiry Date

Dec 03, 2025

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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