Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Mindray, Snap, AHA (UDI 10190752182721)
Manufactured by AirLife Finland Oy
Device Regulatory Overview
The Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Mindray, Snap, AHA (Model/Catalog Number: 2090101-621) is a medical device manufactured by AirLife Finland Oy. This product is indexed under FDA Product Code / Category Classification Z12050385 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2090101-621
- Product Code / EMDN
- Z12050385
- Device Name
- Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set
- Database Sync Date
- 2026-08-09 16:29:55
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Mindray, Snap, AHA?
The registered manufacturer of record for Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Mindray, Snap, AHA is AirLife Finland Oy.
What is the Primary UDI-DI identifier for Multi-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Mindray, Snap, AHA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10190752182721.
What classification code is assigned to this device?
This device is registered under product classification code Z12050385.
Similar Classification Devices (Z12050385)
Other Devices by AirLife Finland Oy
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