Identity
- Trade Name
- Electrode for ABL analyzers FDA UDI
- Generic Name
- Potassium (K+) IVD, kit, ion-selective electrode (ISE) FDA UDI
- Device Name
- E722 K electrode for ABL7XX/8XX FDA UDI
- Model / Reference
- 945-615 FDA UDI
- Description
- E722 K electrode for ABL7XX/8XX FDA UDI
Identifiers
- Catalog Number
- 945-615 FDA UDI
- Primary DI / UDI-DI
- 05700699456151 FDA UDI
- FDA Product Code
- CEM FDA UDIKQI FDA UDICGZ FDA UDIJGS FDA UDICIG FDA UDIMQM FDA UDICHL FDA UDIKHP FDA UDIJFP FDA UDICGA FDA UDIGHS FDA UDICGL FDA UDI
- GMDN Term
- Potassium (K+) IVD, kit, ion-selective electrode (ISE) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1600 FDA UDI864.7455 FDA UDI862.1170 FDA UDI862.1665 FDA UDI862.1110 FDA UDI862.1113 FDA UDI862.1120 FDA UDI862.1450 FDA UDI862.1145 FDA UDI862.1345 FDA UDI864.7425 FDA UDI862.1225 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Potassium (K+) IVD, kit, ion-selective electrode (ISE)
Electrode for ABL analyzers by Radiometer Medical ApS — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Radiometer Medical ApS
Sources (1)
- FDA UDI 594840d5-5ced-4f58-bb2c-f4a97aa412ca 35 fields · synced Jun 6, 2026