Human IgA1 Subclass Kit (for Siemens BN™II) (UDI 05051700007801)
Manufactured by The Binding Site Group Ltd
Device Regulatory Overview
The Human IgA1 Subclass Kit (for Siemens BN™II) (Model/Catalog Number: NK087.1T) is a medical device manufactured by The Binding Site Group Ltd. This product is indexed under FDA Product Code / Category Classification W0102010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- NK087.1T
- Product Code / EMDN
- W0102010102
- Device Name
- Human IgA1 Subclass Kit (for Siemens BN™II)
- Database Sync Date
- 2026-08-09 17:51:20
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Human IgA1 Subclass Kit (for Siemens BN™II)?
The registered manufacturer of record for Human IgA1 Subclass Kit (for Siemens BN™II) is The Binding Site Group Ltd.
What is the Primary UDI-DI identifier for Human IgA1 Subclass Kit (for Siemens BN™II)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051700007801.
What classification code is assigned to this device?
This device is registered under product classification code W0102010102.
Similar Classification Devices (W0102010102)
Other Devices by The Binding Site Group Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint