Human Complement C5 NL BINDARID™ Kit (UDI 05051700010603)
Manufactured by The Binding Site Group Ltd
Device Regulatory Overview
The Human Complement C5 NL BINDARID™ Kit (Model/Catalog Number: RN027.3) is a medical device manufactured by The Binding Site Group Ltd. This product is indexed under FDA Product Code / Category Classification W0102010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RN027.3
- Product Code / EMDN
- W0102010299
- Device Name
- Human Complement C5 NL BINDARID™ Kit
- Database Sync Date
- 2026-08-09 16:49:31
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 Human Complement C5 NL BINDARID™ Kit?
The registered manufacturer of record for Human Complement C5 NL BINDARID™ Kit is The Binding Site Group Ltd.
What is the Primary UDI-DI identifier for Human Complement C5 NL BINDARID™ Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051700010603.
What classification code is assigned to this device?
This device is registered under product classification code W0102010299.
Similar Classification Devices (W0102010299)
Other Devices by The Binding Site Group Ltd
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