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Multi-Link™ X2 ECG Reusable Trunk Cable 3-Lead for Nihon Kohden, IEC, 3.6 m/ 12…
EUDAMEDFDA UDIClass I (EU MDR)
Ref 2090200-082
Identity
- Trade Name
- Multi-Link™ X2 ECG Reusable Trunk Cable 3-Lead for Nihon Kohden, IEC, 3.6 m/ 12 ft EUDAMEDMulti-Link™ FDA UDI
- Generic Name
- Electrocardiographic lead set, reusable FDA UDI
- Device Name
- Multi-Link™ X2 ECG Reusable Trunk Cable EUDAMEDX2 ECG Reusable Trunk Cable FDA UDI
- Model / Reference
- 2090200-082 EUDAMEDFDA UDI
- Description
- X2 ECG Reusable Trunk Cable FDA UDI
Identifiers
- Catalog Number
- 2090200-082 FDA UDI
- Primary DI / UDI-DI
- 10190752183063 EUDAMEDFDA UDI
- Basic UDI-DI
- 0190752TDHEL1313UT EUDAMED
- Direct Marketing DI
- 10190752183063 EUDAMED
- FDA Product Code
- DSA FDA UDI
- EMDN Code
- Z12050380 ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Electrocardiographic lead set, reusable 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
No
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
High-level Disinfectant FDA UDI
MR Unsafe FDA UDI
Multi-Link™ X2 ECG Reusable Trunk Cable 3-Lead for Nihon Kohden, IEC, 3.6 m/ 12… 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 | 0190752TDHEL1313UT | 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 348c2ceb-8432-4d42-894f-e6edd80bd3d7 61 fields · synced Jun 18, 2026
- FDA UDI 403910ff-ff3f-4bc7-8d70-0b3ac58a883d 36 fields · synced May 30, 2026