← Back to catalogue

Dimension® Flex® reagent cartridge EC02

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Dimension® Flex® reagent cartridge EC02 FDA UDI
Generic Name
Carbon dioxide (CO2) IVD, kit, spectrophotometry FDA UDI
Device Name
Enzymatic Carbonate Flex® reagent cartridge, 360 tests FDA UDI
Model / Reference
10444972 FDA UDI
Description
Enzymatic Carbonate Flex® reagent cartridge, 360 tests FDA UDI

Identifiers

Catalog Number
DF137 FDA UDI
Primary DI / UDI-DI
00842768005374 FDA UDI
510(k) Number
K010206 FDA UDI
FDA Product Code
KHS FDA UDI
GMDN Term
Carbon dioxide (CO2) IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1160 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: Carbon dioxide (CO2) IVD, kit, spectrophotometry

Dimension® Flex® reagent cartridge EC02 by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide (CO2) IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 0b5ca959-c255-4f7e-a7ab-e6a1f5fecb4c 37 fields · synced Jun 8, 2026