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Atellica CH hsCRP

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Atellica CH hsCRP FDA UDI
Generic Name
C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
High Sensitivity C-Reactive Protein (hsCRP) Atellica CH - RGT 740T FDA UDI
Model / Reference
11097633 FDA UDI
Description
High Sensitivity C-Reactive Protein (hsCRP) Atellica CH - RGT 740T FDA UDI

Identifiers

Catalog Number
11097633 FDA UDI
Primary DI / UDI-DI
00630414596174 FDA UDI
510(k) Number
K081294 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

Atellica CH hsCRP by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 579b7332-35a8-4e69-a64a-1b942bdb358a 37 fields · synced May 30, 2026