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Multi-Link™ ECG Leadwire, 6-lead, Grabber, AHA, 74 cm/29 in & 130 cm/51 in
EUDAMEDFDA UDIClass I (EU MDR)
Ref 421932-003Model Multi-Link ECG leadwires
Identity
- Trade Name
- Multi-Link™ ECG Leadwire, 6-lead, Grabber, AHA, 74 cm/29 in & 130 cm/51 in EUDAMEDMulti-Link™ FDA UDI
- Generic Name
- Electrocardiographic lead set, reusable FDA UDI
- Device Name
- Multi-Link™ ECG Leadwire, 6-lead, Grabber, AHA, 74 cm/29 in & 130 cm/51 in FDA UDI
- Model / Reference
- Multi-Link ECG leadwires EUDAMED421932-003 EUDAMEDFDA UDI
- Description
- Multi-Link™ ECG Leadwire, 6-lead, Grabber, AHA, 74 cm/29 in & 130 cm/51 in FDA UDI
Identifiers
- Catalog Number
- 421932-003 FDA UDI
- Primary DI / UDI-DI
- 10889483583319 EUDAMEDFDA UDI
- Basic UDI-DI
- 088948320041cECGmon138 EUDAMED
- Direct Marketing DI
- 10889483583319 EUDAMED
- 510(k) Number
- K980582 FDA UDI
- 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
MR Unsafe FDA UDI
Multi-Link™ ECG Leadwire, 6-lead, Grabber, AHA, 74 cm/29 in & 130 cm/51 in 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 | 088948320041cECGmon138 | 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 0bae5032-f01f-49b6-8ae2-e1d7d948a379 61 fields · synced Oct 7, 2026
- FDA UDI 51be27c9-d36e-4018-b612-48b3a0840d59 37 fields · synced May 29, 2026