gudid
Primary ID: 1012188-500.DEU
LIGHTSPECS (UDI 1012188-500.DEU)
Manufactured by FGX INTERNATIONAL INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LIGHTSPECS - Primary ID 1012188-500.DEU
Device Regulatory Overview
The LIGHTSPECS (Model/Catalog Number: 1012188-500.DEU) is a medical device manufactured by FGX INTERNATIONAL INC.. This product is indexed under FDA Product Code / Category Classification HOI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1012188-500.DEU
- Product Code / EMDN
- HOI
- Device Name
- Database Sync Date
- 2026-08-09 09:00:32
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 LIGHTSPECS?
The registered manufacturer of record for LIGHTSPECS is FGX INTERNATIONAL INC..
What is the Primary UDI-DI identifier for LIGHTSPECS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1012188-500.DEU.
What classification code is assigned to this device?
This device is registered under product classification code HOI.
Similar Classification Devices (HOI)
Other Devices by FGX INTERNATIONAL INC.
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