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Potassium Test

FDA UDI

Class II (US FDA UDI)

by Stanbio Laboratory, L.p.

Identity

Trade Name
Potassium Test FDA UDI
Generic Name
Potassium (K+) IVD, reagent FDA UDI
Device Name
Quantitative Turbidimetric Determination of Potassium in Serum, Plasma or Urine . FDA UDI
Model / Reference
0160-050 FDA UDI
Description
Quantitative Turbidimetric Determination of Potassium in Serum, Plasma or Urine . FDA UDI

Identifiers

Catalog Number
0160-050 FDA UDI
Primary DI / UDI-DI
00657498000984 FDA UDI
FDA Product Code
CEI FDA UDI
GMDN Term
Potassium (K+) IVD, reagent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1665 FDA UDI
Commercial Distribution
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

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

No

FDA UDI

Category: Potassium (K+) IVD, reagent

Potassium Test by Stanbio Laboratory, L.p. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Potassium (K+) IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 86ec7ba0-978f-4df1-a704-024c90339683 36 fields · synced May 31, 2026