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ADVIA Centaur® CP Immunoassay System

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA Centaur® CP Immunoassay System FDA UDI
Generic Name
Chemiluminescent immunoassay analyser IVD FDA UDI
Device Name
ADVIA® CENTAUR® CP Instrument FDA UDI
Model / Reference
10309710 FDA UDI
Description
ADVIA® CENTAUR® CP Instrument FDA UDI

Identifiers

Catalog Number
086-A002-01 FDA UDI
Primary DI / UDI-DI
00630414523286 FDA UDI
510(k) Number
K041133 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Chemiluminescent immunoassay analyser IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Chemiluminescent immunoassay analyser IVD

ADVIA Centaur® CP Immunoassay System by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chemiluminescent immunoassay analyser IVD.

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 9dd17f76-fbb7-49f5-98a3-e2a0a4d56186 37 fields · synced May 30, 2026