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Dimension® Flex® reagent cartridge CHOL

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Dimension® Flex® reagent cartridge CHOL FDA UDI
Generic Name
Total cholesterol lipid IVD, kit, spectrophotometry FDA UDI
Device Name
Cholesterol Flex® reagent cartridge, 480 tests FDA UDI
Model / Reference
10444891 FDA UDI
Description
Cholesterol Flex® reagent cartridge, 480 tests FDA UDI

Identifiers

Catalog Number
DF27 FDA UDI
Primary DI / UDI-DI
00842768005466 FDA UDI
510(k) Number
K861700 FDA UDI
FDA Product Code
CHH FDA UDI
GMDN Term
Total cholesterol lipid IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1175 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: Total cholesterol lipid IVD, kit, spectrophotometry

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

Similar devices

Also classified as Total cholesterol lipid IVD, kit, spectrophotometry.

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 213ba18e-d9da-4f2f-ac5f-cc65a839f3ae 37 fields · synced Jun 8, 2026