gudid
Primary ID: 06
BostonSight SCLERAL (UDI 06)
Manufactured by The Boston Foundation For Sight, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BostonSight SCLERAL - Primary ID 06
Device Regulatory Overview
The BostonSight SCLERAL (Model/Catalog Number: 06) is a medical device manufactured by The Boston Foundation For Sight, Inc.. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 06
- Product Code / EMDN
- HQD
- Device Name
- BostonSight SCLERAL for daily wear, fabricated from Optimum Extreme (roflufocon E) - Clear- THP coated
- Database Sync Date
- 2026-08-09 09:59:00
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 BostonSight SCLERAL?
The registered manufacturer of record for BostonSight SCLERAL is The Boston Foundation For Sight, Inc..
What is the Primary UDI-DI identifier for BostonSight SCLERAL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by The Boston Foundation For Sight, Inc.
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