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INTRA Hydrophobic Acrylic Foldable IOL - Indonesia BPOM Medical Device Registration

INTRA Hydrophobic Acrylic Foldable IOL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202220031. The device is manufactured by OMNI LENS PVT LTD from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. DOCARE LARAS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
INTRA Hydrophobic Acrylic Foldable IOL
Analysis ID: AKL 31202220031

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

OMNI LENS PVT LTD

Country of Origin

India

Authorized Representative

PT. DOCARE LARAS INDONESIA

AR Address

GRAHA ANTARI, JL. PULO KAMBING NO. 16 KAWASAN INDUSTRI PULO GADUNG

Registration Date

Apr 27, 2022

Expiry Date

Jan 25, 2027

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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