gudid
Primary ID: itafocon B
Boston IV (UDI itafocon B)
Manufactured by Bausch & Lomb Incorporated
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Boston IV - Primary ID itafocon B
Device Regulatory Overview
The Boston IV (Model/Catalog Number: itafocon B) is a medical device manufactured by Bausch & Lomb Incorporated. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- itafocon B
- Product Code / EMDN
- HQD
- Device Name
- Rigid Gas Permeable Contact Lens
- Database Sync Date
- 2026-08-09 09:41:25
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 Boston IV?
The registered manufacturer of record for Boston IV is Bausch & Lomb Incorporated.
What is the Primary UDI-DI identifier for Boston IV?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is itafocon B.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by Bausch & Lomb Incorporated
Programmatic Export
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JSON API Endpoint