Identity
- Trade Name
- Ambu WhiteSensor 4242 FDA UDI
- Generic Name
- Electrocardiographic electrode, single-use FDA UDI
- Device Name
- White Sensor 4242-00-S/50 ECG electrode Wet gel, foam backing and offset connector Pouch 50 pcs. /box 1000 pcs / carton 6000 pcs FDA UDI
- Model / Reference
- 4242-00-S/50 FDA UDI
- Description
- White Sensor 4242-00-S/50 ECG electrode Wet gel, foam backing and offset connector Pouch 50 pcs. /box 1000 pcs / carton 6000 pcs FDA UDI
Identifiers
- Catalog Number
- 4242-00-S/50 FDA UDI
- Primary DI / UDI-DI
- 05707480136766 FDA UDI
- FDA Product Code
- DRX FDA UDI
- GMDN Term
- Electrocardiographic electrode, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2360 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ambu WhiteSensor 4242 by Ambu A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Ambu A/S
Sources (1)
- FDA UDI 8e1325e6-b053-4b84-8eb9-260837921171 37 fields · synced May 31, 2026