Multi-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Snap, IEC
Ref 2090201-521, 2090201-522, 2090201-813, 2090201-611, 2090201-622, 2090201-821, 2090201-511, 2090201-523, 2090201-811, 2090101-823, 2090201-823, 2090201-612, 2090201-513Model Multi-Link X2 Single-Patient-Use Long ECG Leadwire Sets
Active
CE MDR
Valid until
Not listed
FDA recalls
None foundDocuments
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number088948320041cECGmon12XT | Date15 May 2025 | StatusActive |
| United States | GUDID listing GUDID | Number10889483618905 | Date2 Apr 2025 | StatusListed |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Recalls
No FDA recalls found in the data synced 25 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Multi-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Snap, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 5-Lead Set for Philips, Snap, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 6-Lead Set for Nihon Kohden, Grabber, IEC EUDAMEDMulti-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Mindray, Grabber, IEC EUDAMEDMulti-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 5-Lead Set for Mindray, Snap, IEC EUDAMEDMulti-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 5-Lead Set for Philips, Snap, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Nihon Kohden, Snap, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Grabber, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 6-Lead Set for Philips, Snap, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Nihon Kohden, Grabber, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 6-Lead Set for Nihon Kohden, Snap, AHA EUDAMEDMulti-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Nihon Kohden, Snap, IEC EUDAMEDMulti-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 6-Lead Set for Nihon Kohden, Snap, IEC EUDAMEDMulti-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Nihon Kohden, Grabber, IEC EUDAMEDMulti-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 3-Lead Set for Philips, Grabber, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 5-Lead Set for Mindray, Grabber, IEC EUDAMEDMulti-Link™ X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 6-Lead Set for Philips, Grabber, IEC EUDAMEDMulti-LinkTM X2 Single-Patient-Use Direct-Connect Telemetry ECG Leadwire Set 5-Lead Set for Mindray, Snap, IEC EUDAMEDMulti-Link™ GUDID
- Generic Name
- Electrocardiographic lead set, single-use
- Device Name
- Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set
- Model / Ref / Catalog
- Multi-Link X2 Single-Patient-Use Long ECG Leadwire Sets, 2090201-521, 2090201-522, 2090201-813, 2090201-611, 2090201-622, 2090201-821, 2090201-511, 2090201-523, 2090201-811, 2090101-823, 2090201-823, 2090201-612, 2090201-513
- Primary DI / UDI-DI
- 10889483618905, 10889483618912, 10889483618967, 10190752183155, 10190752183186, 10190752183131, 10889483618974, 10889483618875, 10889483618929, 10889483618950, 10889483578032, 10190752183216, 10190752183223, 10190752183193, 10190752183094, 10889483618936, 10190752183117, 10889483618943
- Basic UDI-DI
- 088948320041cECGmon12XT, 0190752TDHEL1312UR
- 510(k) Number
- FDA Product Code
- DSA
- EMDN Code
- Z12050385 Electrocardiographs - consumables
- GMDN Term
- Electrocardiographic lead set, single-use
- Device Class
- Class I EUDAMEDClass II GUDID
- Regulation Number
- 870.2900
- EU market of registration
- Finland
- GUDID distribution status
- In Commercial Distribution
- MRI Safety
- MR Unsafe
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class I | Class II |
Manufacturer details
- EUDAMED SRN
- FI-MF-000001482
Other devices from AirLife Finland Oy
Properties
Other properties (20)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No