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BRILIGHT Single Piece Posterior Chamber Hydrophilic Acrylic - Foldable Aspheric IOL - Indonesia BPOM Medical Device Registration

BRILIGHT Single Piece Posterior Chamber Hydrophilic Acrylic - Foldable Aspheric IOL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320191. The device is manufactured by LIFELINE MEDICAL DEVICES PVT.LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. OPHTHALINDO JAYA MANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : D
BRILIGHT Single Piece Posterior Chamber Hydrophilic Acrylic - Foldable Aspheric IOL
Analysis ID: AKL 31202320191

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

PT. OPHTHALINDO JAYA MANDIRI

AR Address

Superblock Mega Kemayoran (MGK) Blok A No. 8-9 Jl. Angkasa Kav. B-6, Kota Baru, Bandar Kemayoran, Kode Pos 10610, Kel. Gunung Sahari Selatan, Kec. Kemayoran, Kota Jakarta Pusat, Prov. DKI Jakarta

Registration Date

Dec 28, 2023

Expiry Date

May 26, 2028

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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