Identity
- Trade Name
- Potassium Electrode FDA UDI
- Generic Name
- Potassium (K+) IVD, kit, ion-selective electrode (ISE) FDA UDI
- Model / Reference
- 279-001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03701700829256 FDA UDI
- GMDN Term
- Potassium (K+) IVD, kit, ion-selective electrode (ISE) FDA UDI
Classification
- 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
Yes
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
Category: Potassium (K+) IVD, kit, ion-selective electrode (ISE)
Potassium Electrode by Vitalscientific — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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- Membrane for E722 electrode — Radiometer Medical ApS · Class II
- Potassium electrode — Roche Diagnostics Corp. · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
IVDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | IVDR | — | N/A | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | N/A | Pending data |
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Manufacturer
- Manufacturer
- Vitalscientific
Sources (2)
- FDA UDI 3dbb6841-40c1-4bfc-9a91-e999450afdc1 32 fields · synced Jun 18, 2026
- EUDAMED 1 fields · synced Jun 3, 2026