eudamed_udi
Primary ID: 05051700017053
Optilite® C4 Kit (UDI 05051700017053)
Manufactured by The Binding Site Group Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Optilite® C4 Kit - Primary ID 05051700017053
Device Regulatory Overview
The Optilite® C4 Kit (Model/Catalog Number: NK025.OPT) is a medical device manufactured by The Binding Site Group Ltd. This product is indexed under FDA Product Code / Category Classification W0102010205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NK025.OPT
- Product Code / EMDN
- W0102010205
- Device Name
- Optilite® C4 Kit
- Database Sync Date
- 2026-08-09 17:35:01
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 Optilite® C4 Kit?
The registered manufacturer of record for Optilite® C4 Kit is The Binding Site Group Ltd.
What is the Primary UDI-DI identifier for Optilite® C4 Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051700017053.
What classification code is assigned to this device?
This device is registered under product classification code W0102010205.
Similar Classification Devices (W0102010205)
Other Devices by The Binding Site Group Ltd
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