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Dimension Vista® Flex® reagent cartridge LAMBDA

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
Dimension Vista® Flex® reagent cartridge LAMBDA FDA UDI
Generic Name
Kappa/lambda light chain immunoglobulin IVD, kit, nephelometry/turbidimetry FDA UDI
Device Name
For the quantitative measurement of immunoglobulin light chains, type lambda in human serum and plasma on the Dimension Vista® System FDA UDI
Model / Reference
10465672 FDA UDI
Description
For the quantitative measurement of immunoglobulin light chains, type lambda in human serum and plasma on the Dimension Vista® System FDA UDI

Identifiers

Catalog Number
K7051 FDA UDI
Primary DI / UDI-DI
00842768024436 FDA UDI
510(k) Number
K082503 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

Dimension Vista® Flex® reagent cartridge LAMBDA by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID

Similar devices

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

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 a8601f77-5165-42ad-882d-9a6852d43ee2 37 fields · synced Jun 8, 2026