Multi-Link™ X2 ECG Reusable Telemetry Adapter 3-Lead for Nihon Kohden
by AirLife Finland Oy EUDAMEDGUDID
Active
Ref 2090101-080
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0190752TDHEL1314UV | Date15 Dec 2021 | StatusActive |
| United States | GUDID listing GUDID | Number10190752182523 | Date22 Dec 2020 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.
Recalls
No FDA recalls on record, checked 24 Oct 2026.
Specification
- Trade Name
- Multi-Link™ X2 ECG Reusable Telemetry Adapter 3-Lead for Nihon Kohden EUDAMEDMulti-Link™ GUDID
- Generic Name
- Electrocardiographic lead set, reusable
- Model / Ref / Catalog
- 2090101-080
- Primary DI / UDI-DI
- 10190752182523
- Basic UDI-DI
- 0190752TDHEL1314UV
- Direct Marketing DI
- 10190752182523
- FDA Product Code
- DSA
- EMDN Code
- Z12050380 Electrocardiographs - hardware accessories
- GMDN Term
- Electrocardiographic lead set, reusable
- Device Class
- Class I EUDAMEDClass II GUDID
- Regulation Number
- 870.2900
- Market of Registration
- Finland
- Commercial Distribution
- 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 (21)
- Sterile: No
- Single Use: 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