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N Latex Flc Kappa

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
N LATEX FLC KAPPA FDA UDI
Generic Name
Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
Quantitative determination of free light chains (FLC) type kappa in human serum and EDTA-plasma on Siemens analyzers FDA UDI
Model / Reference
10873629 FDA UDI
Description
Quantitative determination of free light chains (FLC) type kappa in human serum and EDTA-plasma on Siemens analyzers FDA UDI

Identifiers

Catalog Number
OPJA075 FDA UDI
Primary DI / UDI-DI
00630414167657 FDA UDI
FDA Product Code
DFH FDA UDI
GMDN Term
Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5550 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: Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry

N Latex Flc Kappa by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI b2c1a2ac-43b1-49b0-9a9b-5830bd6338c2 36 fields · synced Jun 8, 2026