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ADVIA Centaur® VB12

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA Centaur® VB12 FDA UDI
Generic Name
Vitamin B12 IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
Vitamin B12 - CENTAUR - RGT - 100 tests FDA UDI
Model / Reference
10309970 FDA UDI
Description
Vitamin B12 - CENTAUR - RGT - 100 tests FDA UDI

Identifiers

Catalog Number
110747 FDA UDI
Primary DI / UDI-DI
00630414177168 FDA UDI
510(k) Number
K993571 FDA UDI
FDA Product Code
CDD FDA UDI
GMDN Term
Vitamin B12 IVD, kit, chemiluminescent immunoassay FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1810 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: Vitamin B12 IVD, kit, chemiluminescent immunoassay

ADVIA Centaur® VB12 by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vitamin B12 IVD, kit, chemiluminescent immunoassay.

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 1948539d-d621-48e6-afb0-e056421018da 37 fields · synced May 30, 2026