Unit Connection Cable, 10M YS-107P4
EUDAMEDFDA UDIClass I (EU MDR)
Identity
- Trade Name
- Unit Connection Cable, 10M YS-107P4 EUDAMEDConnection Cable 10m EUDAMEDNA FDA UDI
- Generic Name
- General-purpose multi-parameter bedside monitor FDA UDI
- Device Name
- General-purpose multi-parameter bedside monitor EUDAMEDElectrocardiograph, professional, multichannel EUDAMEDUnit Connection Cable - G9 DAU FDA UDI
- Model / Reference
- YS-107P4 EUDAMEDFDA UDIK117F EUDAMED
- Description
- Unit Connection Cable - G9 DAU FDA UDI
Identifiers
- Catalog Number
- YS-107P4 FDA UDI
- Primary DI / UDI-DI
- 04931921112519 EUDAMEDFDA UDI04931921903834 EUDAMED
- Basic UDI-DI
- 4931921MD10004BD EUDAMED4931921MD10015BJ EUDAMED
- FDA Product Code
- MHX FDA UDI
- EMDN Code
- Z1203020285 MULTI-PARAMETER MONITORS - CONSUMABLES EUDAMEDZ12050385 ELECTROCARDIOGRAPHS - CONSUMABLES EUDAMED
- GMDN Term
- General-purpose multi-parameter bedside monitor FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1025 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
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
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
No
Manufacturing Date
No
Category: General-purpose multi-parameter bedside monitor
Unit Connection Cable, 10M YS-107P4 by Nihon Kohden Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 4931921MD10004BD | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Nihon Kohden Corporation
- EUDAMED SRN
- JP-MF-000019022
- Authorised Representative
- NIHON KOHDEN EUROPE GmbH DE-AR-000010740
Sources (3)
- EUDAMED cb98e426-e1da-48ca-9729-be52450450ba 61 fields · synced Oct 6, 2026
- FDA UDI 825e2888-2f60-46e6-b048-22b203675432 35 fields · synced May 30, 2026
- EUDAMED 029c3f7d-f4ca-4d48-b315-af6cad4ae2ad 61 fields · synced Jul 18, 2026