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C-Saa Analyt Module Assy 2120i

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
C-SAA ANALYT MODULE ASSY 2120I FDA UDI
Generic Name
Haematological cell analyser IVD FDA UDI
Device Name
ADVIA 2120i Refurbished System, Single Aspirate FDA UDI
Model / Reference
11314044 FDA UDI
Description
ADVIA 2120i Refurbished System, Single Aspirate FDA UDI

Identifiers

Catalog Number
11314044 FDA UDI
Primary DI / UDI-DI
00630414237879 FDA UDI
510(k) Number
K162977 FDA UDI
FDA Product Code
GKZ FDA UDI
GMDN Term
Haematological cell analyser IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5220 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Haematological cell analyser IVD

C-Saa Analyt Module Assy 2120i by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haematological cell 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 e4f5745b-2195-40a6-baa2-ef4697aad1fa 36 fields · synced Jun 8, 2026