Pure Global

C-THRU Hydrophilic Acrylic Foldable IOL - Indonesia BPOM Medical Device Registration

C-THRU Hydrophilic Acrylic Foldable IOL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320134. 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. VISIMED GLOBAL STANDALONE.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : D
C-THRU Hydrophilic Acrylic Foldable IOL
Analysis ID: AKL 31202320134

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

PT. VISIMED GLOBAL STANDALONE

AR Address

VISIMED GLOBAL MANDIRI

Registration Date

Aug 18, 2023

Expiry Date

Feb 13, 2028

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from PT. VISIMED GLOBAL STANDALONE
Products with the same authorized representative (2 products)