Identity
- Trade Name
- ADULT FOAM ECG ELECTRODE, DISPOSABLE EUDAMEDECG Electrodes FDA UDI
- Generic Name
- Electrocardiographic electrode, single-use FDA UDI
- Device Name
- Electrocardiographic Electrodes EUDAMEDAdult Foam ECG Electrode, Disposable Silver/silver-chloride sensor. Pre-gelled. 54 mm diameter. 5 electrodes/pack, 15 packs/box, 4 boxes/case, 300 electrodes/case. FDA UDI
- Model / Reference
- 40493D EUDAMEDADULT FOAM ECG ELECTRODE, DISPOSABLE FDA UDI
- Description
- Adult Foam ECG Electrode, Disposable Silver/silver-chloride sensor. Pre-gelled. 54 mm diameter. 5 electrodes/pack, 15 packs/box, 4 boxes/case, 300 electrodes/case. FDA UDI
Identifiers
- Catalog Number
- 40493D FDA UDI
- Primary DI / UDI-DI
- 20884838007127 EUDAMEDFDA UDI
- Basic UDI-DI
- 0884838BM340SM EUDAMED
- Unit of Use DI
- 10884838007120 EUDAMED
- FDA Product Code
- DRX FDA UDI
- EMDN Code
- Z1203020202 TRANSPORTABLE/PORTABLE MULTI–PARAMETER PATIENT MONITORS EUDAMED
- GMDN Term
- Electrocardiographic electrode, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.2360 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Adult Foam Ecg Electrode, Disposable by Philips Medical Systems — 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 | 0884838BM340SM | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Philips Medical Systems
- EUDAMED SRN
- US-MF-000002321
- Authorised Representative
- Philips Medical Systems Nederland B.V. NL-AR-000001422
Sources (2)
- EUDAMED b04597b0-a37f-4f1b-91b1-f614862152ff 61 fields · synced Jul 9, 2026
- FDA UDI 9cd83d1d-15a2-4822-a4cb-c6e08449051b 36 fields · synced May 30, 2026