Freelite® Human Lambda Free Kit (for use on the Siemens BN™II) (UDI 05051700006491)
Manufactured by The Binding Site Group Ltd
Device Regulatory Overview
The Freelite® Human Lambda Free Kit (for use on the Siemens BN™II) (Model/Catalog Number: LK018.T) is a medical device manufactured by The Binding Site Group Ltd. This product is indexed under FDA Product Code / Category Classification W0102010109 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LK018.T
- Product Code / EMDN
- W0102010109
- Device Name
- Freelite® Human Lambda Free Kit (for use on the Siemens BN™II)
- Database Sync Date
- 2026-08-09 17:35:13
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 Freelite® Human Lambda Free Kit (for use on the Siemens BN™II)?
The registered manufacturer of record for Freelite® Human Lambda Free Kit (for use on the Siemens BN™II) is The Binding Site Group Ltd.
What is the Primary UDI-DI identifier for Freelite® Human Lambda Free Kit (for use on the Siemens BN™II)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051700006491.
What classification code is assigned to this device?
This device is registered under product classification code W0102010109.
Similar Classification Devices (W0102010109)
Other Devices by The Binding Site Group Ltd
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