Identity
- Trade Name
- Wide ECG 3.0 Cable IEC EUDAMEDMR Patient Care Wide ECG 3.0 Cable IEC FDA UDI
- Generic Name
- Electrocardiographic lead set, reusable FDA UDI
- Device Name
- Reusable Electrocardiographic Leads EUDAMEDECG lead cable designed for use with 3rd-generation wireless ECG module and CV Quadtrodes (IEC coded leads.) FDA UDI
- Model / Reference
- 989803193751 EUDAMEDWide ECG 3.0 Cable IEC FDA UDI
- Description
- ECG lead cable designed for use with 3rd-generation wireless ECG module and CV Quadtrodes (IEC coded leads.) FDA UDI
Identifiers
- Catalog Number
- 989803193751 FDA UDI
- Primary DI / UDI-DI
- 00884838121157 EUDAMEDFDA UDI
- Basic UDI-DI
- 0884838BM1072M2 EUDAMED
- Direct Marketing DI
- 00884838121157 EUDAMED
- FDA Product Code
- MWI FDA UDI
- EMDN Code
- Z1203020299 MULTI–PARAMETER MONITORS - OTHER EUDAMED
- GMDN Term
- Electrocardiographic lead set, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.2300 FDA UDI
- Market of Registration
- Austria 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
No
FDA UDI
MR Conditional FDA UDI
Wide ECG 3.0 Cable IEC by Philips Medizin Systeme Böblingen GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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 | 0884838BM1072M2 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Philips Medizin Systeme Böblingen GmbH
- EUDAMED SRN
- DE-MF-000006026
Sources (2)
- EUDAMED 0d8cd05d-c6b0-4418-ad37-0d6adcfd5862 61 fields · synced Jun 18, 2026
- FDA UDI a4aa73ce-b6e8-4b21-9a20-9e7e4b4dc649 35 fields · synced May 30, 2026