Multi-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Snap, AHA (UDI 10889483577936)
Manufactured by AirLife Finland Oy
Device Regulatory Overview
The Multi-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Snap, AHA (Model/Catalog Number: 2090101-521) 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
- 2090101-521
- Product Code / EMDN
- Z12050385
- Device Name
- Multi-Link X2 Single-Patient-Use Long ECG Leadwire Sets
- Database Sync Date
- 2026-08-09 16:30:37
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-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Snap, AHA?
The registered manufacturer of record for Multi-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Snap, AHA is AirLife Finland Oy.
What is the Primary UDI-DI identifier for Multi-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Snap, AHA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10889483577936.
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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