Optilite® C3c Control Pack (UDI 05051700019156)
Manufactured by The Binding Site Group Ltd
Device Regulatory Overview
The Optilite® C3c Control Pack (Model/Catalog Number: NQ023.OPT) is a medical device manufactured by The Binding Site Group Ltd. This product is indexed under FDA Product Code / Category Classification W0102010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NQ023.OPT
- Product Code / EMDN
- W0102010203
- Device Name
- Optilite® C3c Kit
- Database Sync Date
- 2026-08-09 17:57:50
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® C3c Control Pack?
The registered manufacturer of record for Optilite® C3c Control Pack is The Binding Site Group Ltd.
What is the Primary UDI-DI identifier for Optilite® C3c Control Pack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051700019156.
What classification code is assigned to this device?
This device is registered under product classification code W0102010203.
Similar Classification Devices (W0102010203)
Other Devices by The Binding Site Group Ltd
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