gudid
Primary ID: roflufocon E
Optimum Extreme (UDI roflufocon E)
Manufactured by CONTAMAC HOLDINGS LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Optimum Extreme - Primary ID roflufocon E
Device Regulatory Overview
The Optimum Extreme (Model/Catalog Number: roflufocon E) is a medical device manufactured by CONTAMAC HOLDINGS LIMITED. This product is indexed under FDA Product Code / Category Classification HQD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- roflufocon E
- Product Code / EMDN
- HQD
- Device Name
- Rigid Gas Permeable Contact Lens
- Database Sync Date
- 2026-08-09 09:49:14
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 Optimum Extreme?
The registered manufacturer of record for Optimum Extreme is CONTAMAC HOLDINGS LIMITED.
What is the Primary UDI-DI identifier for Optimum Extreme?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is roflufocon E.
What classification code is assigned to this device?
This device is registered under product classification code HQD.
Similar Classification Devices (HQD)
Other Devices by CONTAMAC HOLDINGS LIMITED
Programmatic Export
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