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Dimension Vista hsCRP Flex reagent cartridge

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
Dimension Vista hsCRP Flex reagent cartridge FDA UDI
Generic Name
C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
For the quantitative measurement of C-reactive protein in human serum and plasma on the Dimension Vista® System FDA UDI
Model / Reference
10445898 FDA UDI
Description
For the quantitative measurement of C-reactive protein in human serum and plasma on the Dimension Vista® System FDA UDI

Identifiers

Catalog Number
K7046 FDA UDI
Primary DI / UDI-DI
00842768006135 FDA UDI
510(k) Number
K061802 FDA UDI
FDA Product Code
NQD FDA UDI
GMDN Term
C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5270 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: C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry

Dimension Vista hsCRP Flex reagent cartridge by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry.

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 cbabaa6d-54cb-40ff-b938-e644e7320c8c 37 fields · synced May 31, 2026