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RAPIDLab® Na+/K+/Ca++/Cl- Electrode Fill

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
RAPIDLab® Na+/K+/Ca++/Cl- Electrode Fill FDA UDI
Generic Name
Multiple electrolyte IVD, kit, ion-selective electrode (ISE) FDA UDI
Device Name
RAPIDLab® Na+/K+/Ca++/Cl- Electrode Fill Solution for in vitro diagnostic use on RAPIDLab® 348/348EX analyzers FDA UDI
Model / Reference
10311047 FDA UDI
Description
RAPIDLab® Na+/K+/Ca++/Cl- Electrode Fill Solution for in vitro diagnostic use on RAPIDLab® 348/348EX analyzers FDA UDI

Identifiers

Catalog Number
478535 FDA UDI
Primary DI / UDI-DI
00630414194455 FDA UDI
510(k) Number
K935830 FDA UDI
FDA Product Code
CHL FDA UDI
GMDN Term
Multiple electrolyte IVD, kit, ion-selective electrode (ISE) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1120 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple electrolyte IVD, kit, ion-selective electrode (ISE)

RAPIDLab® Na+/K+/Ca++/Cl- Electrode Fill by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple electrolyte IVD, kit, ion-selective electrode (ISE).

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 37097b2f-f2d5-4822-b5e5-ae7e8d190487 37 fields · synced May 30, 2026