GUDIDData
eudamed_udi Primary ID: 05050649109171

BMK2 (UDI 05050649109171)

Manufactured by Blatchford Products Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BMK2 - Primary ID 05050649109171

Device Regulatory Overview

The BMK2 (Model/Catalog Number: BMK2) is a medical device manufactured by Blatchford Products Limited. This product is indexed under FDA Product Code / Category Classification Y062415 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BMK2
Product Code / EMDN
Y062415
Device Name
BMK2
Database Sync Date
2026-08-09 16:28:52

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 BMK2?

The registered manufacturer of record for BMK2 is Blatchford Products Limited.

What is the Primary UDI-DI identifier for BMK2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05050649109171.

What classification code is assigned to this device?

This device is registered under product classification code Y062415.

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