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Dimension® Flex® reagent cartridge SAL

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Dimension® Flex® reagent cartridge SAL FDA UDI
Generic Name
Salicylate IVD, kit, spectrophotometry FDA UDI
Device Name
Salicylate Flex® reagent cartridge, 120 tests FDA UDI
Model / Reference
10444915 FDA UDI
Description
Salicylate Flex® reagent cartridge, 120 tests FDA UDI

Identifiers

Catalog Number
DF20 FDA UDI
Primary DI / UDI-DI
00842768005435 FDA UDI
510(k) Number
K904301 FDA UDI
FDA Product Code
DKJ FDA UDI
GMDN Term
Salicylate IVD, kit, spectrophotometry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3830 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: Salicylate IVD, kit, spectrophotometry

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

Similar devices

Also classified as Salicylate IVD, kit, spectrophotometry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare Diagnostics

Sources (1)

  • FDA UDI 183129ff-dfa0-433c-894d-92bd6433c58d 37 fields · synced May 30, 2026