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ADVIA Centaur® Acid Base Reagents

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA Centaur® Acid Base Reagents FDA UDI
Generic Name
Chemiluminescent immunoassay signal generation kit IVD FDA UDI
Device Name
ADVIA Centaur® Acid/Base Reagents FDA UDI
Model / Reference
10310026 FDA UDI
Description
ADVIA Centaur® Acid/Base Reagents FDA UDI

Identifiers

Catalog Number
112219 FDA UDI
Primary DI / UDI-DI
00630414190860 FDA UDI
510(k) Number
K041133 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Chemiluminescent immunoassay signal generation kit 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

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: Chemiluminescent immunoassay signal generation kit IVD

ADVIA Centaur® Acid Base Reagents by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chemiluminescent immunoassay signal generation kit 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 8e6d4019-8f9f-4f5d-82c3-ed5cdce35799 37 fields · synced May 30, 2026