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Dimension® Flex® reagent cartridge THEO

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Dimension® Flex® reagent cartridge THEO FDA UDI
Generic Name
Theophylline therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Theophylline Flex® reagent cartridge, 80 tests FDA UDI
Model / Reference
10444942 FDA UDI
Description
Theophylline Flex® reagent cartridge, 80 tests FDA UDI

Identifiers

Catalog Number
DF71 FDA UDI
Primary DI / UDI-DI
00842768005664 FDA UDI
510(k) Number
K862955 FDA UDI
FDA Product Code
KLS FDA UDI
GMDN Term
Theophylline therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.3880 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: Theophylline therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry

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

Similar devices

Also classified as Theophylline therapeutic drug monitoring IVD, kit, nephelometry/turbidimetry.

Cleared under the same submission

K862955 also covers:

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 0ea6c2f6-d791-406a-88ea-c6bc0712bbf4 37 fields · synced Jun 8, 2026