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ADVIA Centaur® Cuvettes

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA Centaur® Cuvettes FDA UDI
Generic Name
Laboratory analyser cuvette IVD, single-use FDA UDI
Device Name
Laboratory analyser cuvette, IVD FDA UDI
Model / Reference
10309546 FDA UDI
Description
Laboratory analyser cuvette, IVD FDA UDI

Identifiers

Catalog Number
078-K138-01 FDA UDI
Primary DI / UDI-DI
00630414221588 FDA UDI
FDA Product Code
JRI FDA UDI
GMDN Term
Laboratory analyser cuvette IVD, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Laboratory analyser cuvette IVD, single-use

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

Similar devices

Also classified as Laboratory analyser cuvette IVD, single-use.

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 c4e818ff-d50e-4bdf-87b6-5ef3f12a3572 35 fields · synced Jun 8, 2026