Identity
- Trade Name
- Alfa Wassermann FDA UDI
- Generic Name
- Potassium (K+) electrode IVD FDA UDI
- Device Name
- Electrode, Potassium FDA UDI
- Model / Reference
- 903394 FDA UDI
- Description
- Electrode, Potassium FDA UDI
Identifiers
- Catalog Number
- 903394 FDA UDI
- Primary DI / UDI-DI
- 00857969006044 FDA UDI
- FDA Product Code
- CEM FDA UDI
- GMDN Term
- Potassium (K+) electrode IVD FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1600 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
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Potassium (K+) electrode IVD
Alfa Wassermann by Alfa Wassermann, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- I.S.E. K — Randox Laboratories, Ltd. · Class II
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
- Alfa Wassermann, Inc.
Sources (1)
- FDA UDI 573b4def-7cb4-4aa2-9504-72f7af97da53 36 fields · synced May 30, 2026