gudid
Primary ID: +24.0 D
IC-8 Apthera IOL (UDI +24.0 D)
Manufactured by Bausch & Lomb Incorporated
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IC-8 Apthera IOL - Primary ID +24.0 D
Device Regulatory Overview
The IC-8 Apthera IOL (Model/Catalog Number: +24.0 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
- +24.0 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
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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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 +24.0 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
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