CK - MB (UDI 08034063843153)

Manufactured by FAR Srl

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CK - MB (Model/Catalog Number: CL18-75) is a medical device manufactured by FAR Srl. This product is indexed under FDA Product Code / Category Classification W01010114 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CL18-75
Product Code / EMDN: W01010114
Device Name: CK-MB
Database Sync Date: 2026-08-09 17:50:57

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 CK - MB?

The registered manufacturer of record for CK - MB is FAR Srl.

What is the Primary UDI-DI identifier for CK - MB?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08034063843153.

What classification code is assigned to this device?

This device is registered under product classification code W01010114.

Similar Classification Devices (W01010114)

Other Devices by FAR Srl

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