gudid
Primary ID: petrafocon A hem-larafilcon A
SynergEyes casted button (UDI petrafocon A hem-larafilcon A)
Manufactured by SYNERGEYES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SynergEyes casted button - Primary ID petrafocon A hem-larafilcon A
Device Regulatory Overview
The SynergEyes casted button (Model/Catalog Number: petrafocon A hem-larafilcon A) is a medical device manufactured by SYNERGEYES, INC.. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- petrafocon A hem-larafilcon A
- Product Code / EMDN
- HQD
- Device Name
- SynergEyes petrafocon A hem-larafilcon A casted button for Hybrid Contact Lenses
- Database Sync Date
- 2026-08-09 09:16:45
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 SynergEyes casted button?
The registered manufacturer of record for SynergEyes casted button is SYNERGEYES, INC..
What is the Primary UDI-DI identifier for SynergEyes casted button?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is petrafocon A hem-larafilcon A.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by SYNERGEYES, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint