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Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set V-Lead Set, Grabber, AH…
EUDAMEDFDA UDIClass I (EU MDR)
Ref 2052133-408
Identity
- Trade Name
- Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set V-Lead Set, Grabber, AHA, 3.6 m/12 ft EUDAMEDMulti-Link™ FDA UDI
- Generic Name
- Electrocardiographic lead set, single-use FDA UDI
- Device Name
- Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set EUDAMEDMulti-Link™ X2 Single-Patient-Use Long ECG Leadwire Set, V-Lead Set, Grabber, AHA, 3.6 m/12 ft FDA UDI
- Model / Reference
- 2052133-408 EUDAMEDFDA UDI
- Description
- Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set, V-Lead Set, Grabber, AHA, 3.6 m/12 ft FDA UDI
Identifiers
- Catalog Number
- 2052133-408 FDA UDI
- Primary DI / UDI-DI
- 10190752182325 EUDAMEDFDA UDI
- Basic UDI-DI
- 0190752TDHEL1312UR EUDAMED
- FDA Product Code
- DSA FDA UDI
- EMDN Code
- Z12050385 ELECTROCARDIOGRAPHS - CONSUMABLES EUDAMED
- GMDN Term
- Electrocardiographic lead set, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.2900 FDA UDI
- Market of Registration
- Finland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Multi-Link™ X2 Single-Patient-Use Long ECG Leadwire Set V-Lead Set, Grabber, AH… by AirLife Finland Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0190752TDHEL1312UR | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- AirLife Finland Oy
- EUDAMED SRN
- FI-MF-000001482
Sources (2)
- EUDAMED c6335b6a-6d2e-490f-baa2-cbd38943759b 61 fields · synced Oct 6, 2026
- FDA UDI c31624f9-e550-4c83-93d7-a59abbcb87de 36 fields · synced May 29, 2026