gudid Primary ID: +20.0 D

IC-8 Apthera IOL (UDI +20.0 D)

Manufactured by Bausch & Lomb Incorporated

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The IC-8 Apthera IOL (Model/Catalog Number: +20.0 D) is a medical device manufactured by Bausch & Lomb Incorporated. This product is indexed under FDA Product Code / Category Classification POE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: +20.0 D
Product Code / EMDN: POE
Device Name: One-piece UV blocking, hydrophobic acrylic small aperture intraocular lens.
Database Sync Date: 2026-08-09 09:43:35

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of IC-8 Apthera IOL?

The registered manufacturer of record for IC-8 Apthera IOL is Bausch & Lomb Incorporated.

What is the Primary UDI-DI identifier for IC-8 Apthera IOL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +20.0 D.

What classification code is assigned to this device?

This device is registered under product classification code POE.

Similar Classification Devices (POE)

Other Devices by Bausch & Lomb Incorporated

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint