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OP-FOLD Hydrophilic Acrylic Foldable Intraocular Lens - Indonesia BPOM Medical Device Registration

OP-FOLD Hydrophilic Acrylic Foldable Intraocular Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202917868. The device is manufactured by M/S. EXCELLENT HI CARE PVT. LTD from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is YOTA MEDIKA INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
OP-FOLD Hydrophilic Acrylic Foldable Intraocular Lens
Analysis ID: AKL 31202917868

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

YOTA MEDIKA INDONESIA

AR Address

Ruko PulogadungTrade Center Blok 8-A No. 3 Lantai 1&2, Jl. Raya Bekasi KM 21

Registration Date

Dec 09, 2019

Expiry Date

Mar 18, 2024

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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