Optilite® IgM CSF Control Pack (UDI 05051700019019)
Manufactured by The Binding Site Group Ltd
Device Regulatory Overview
The Optilite® IgM CSF Control Pack (Model/Catalog Number: NQ012.L.OPT) is a medical device manufactured by The Binding Site Group Ltd. This product is indexed under FDA Product Code / Category Classification W0102010107 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NQ012.L.OPT
- Product Code / EMDN
- W0102010107
- Device Name
- Optilite® IgM CSF Kit
- Database Sync Date
- 2026-08-09 17:42:35
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® IgM CSF Control Pack?
The registered manufacturer of record for Optilite® IgM CSF Control Pack is The Binding Site Group Ltd.
What is the Primary UDI-DI identifier for Optilite® IgM CSF Control Pack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051700019019.
What classification code is assigned to this device?
This device is registered under product classification code W0102010107.
Similar Classification Devices (W0102010107)
Other Devices by The Binding Site Group Ltd
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