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

I-PURE FOLD Hydrophilic Acrylic Foldable Intraocular Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202024150. The device is manufactured by EXCELLENT HI CARE PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. YOTA MEDIKA INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
I-PURE FOLD Hydrophilic Acrylic Foldable Intraocular Lens
Analysis ID: AKL 31202024150

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

PT. YOTA MEDIKA INDONESIA

AR Address

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

Registration Date

Jul 27, 2020

Expiry Date

Mar 12, 2025

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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