gudid Primary ID: 211-A10050

Pattern MCP 50 (UDI 211-A10050)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Pattern MCP 50 (Model/Catalog Number: 211-A10050) is a medical device manufactured by Keri Medical SA. This product is indexed under FDA Product Code / Category Classification LXH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 211-A10050
Product Code / EMDN: LXH
Device Name
Database Sync Date: 2026-08-09 09:16:08

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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Frequently Asked Questions

Who is the primary manufacturer of Pattern MCP 50?

The registered manufacturer of record for Pattern MCP 50 is Keri Medical SA.

What is the Primary UDI-DI identifier for Pattern MCP 50?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 211-A10050.

What classification code is assigned to this device?

This device is registered under product classification code LXH.

Similar Classification Devices (LXH)

Other Devices by Keri Medical SA

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