GUDIDData
eudamed_udi Primary ID: 05051700006170

Human IgG4 Subclass (Latex) Bulk Kit (for Siemens BN™II) (UDI 05051700006170)

Manufactured by The Binding Site Group Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Human IgG4 Subclass (Latex) Bulk Kit (for Siemens BN™II) - Primary ID 05051700006170

Device Regulatory Overview

The Human IgG4 Subclass (Latex) Bulk Kit (for Siemens BN™II) (Model/Catalog Number: LK009.2TB) is a medical device manufactured by The Binding Site Group Ltd. This product is indexed under FDA Product Code / Category Classification W0102010106 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
LK009.2TB
Product Code / EMDN
W0102010106
Device Name
Human IgG4 Subclass (Latex) Bulk Kit (for Siemens BN™II)
Database Sync Date
2026-08-09 16:50:47

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Human IgG4 Subclass (Latex) Bulk Kit (for Siemens BN™II)?

The registered manufacturer of record for Human IgG4 Subclass (Latex) Bulk Kit (for Siemens BN™II) is The Binding Site Group Ltd.

What is the Primary UDI-DI identifier for Human IgG4 Subclass (Latex) Bulk Kit (for Siemens BN™II)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051700006170.

What classification code is assigned to this device?

This device is registered under product classification code W0102010106.

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