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Sensor Module Cl-

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Sensor Module Cl- FDA UDI
Generic Name
Multiple electrolyte IVD, kit, ion-selective electrode (ISE) FDA UDI
Device Name
Cl- Sensor module an in vitro diagnostics device to be used on the RAPIDChem® 744 analyzer FDA UDI
Model / Reference
10309086 FDA UDI
Description
Cl- Sensor module an in vitro diagnostics device to be used on the RAPIDChem® 744 analyzer FDA UDI

Identifiers

Catalog Number
5453710 FDA UDI
Primary DI / UDI-DI
00630414452135 FDA UDI
510(k) Number
K000926 FDA UDI
FDA Product Code
JGS FDA UDI
CGZ FDA UDI
CEM FDA UDI
GMDN Term
Multiple electrolyte IVD, kit, ion-selective electrode (ISE) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1665 FDA UDI
862.1170 FDA UDI
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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Sensor Module Cl- 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 17f46c29-8149-46f4-86fe-5e4940a94602 36 fields · synced Jun 1, 2026