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Potassium Electrode

FDA UDIEUDAMED

by Vitalscientific

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

Similar devices

Also classified as Potassium (K+) IVD, kit, ion-selective electrode (ISE).

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

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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