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Lambda-PE

FDA UDI

Class I (US FDA UDI)

by Cytognos Sl

Identity

Trade Name
Lambda-PE FDA UDI
Generic Name
Kappa/lambda light chain immunoglobulin IVD, antibody FDA UDI
Device Name
Lambda-PE FDA UDI
Model / Reference
CYT-LAMBPE-A FDA UDI
Description
Lambda-PE FDA UDI

Identifiers

Catalog Number
CYT-LAMBPE-A FDA UDI
Primary DI / UDI-DI
08436548983659 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Kappa/lambda light chain immunoglobulin IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Kappa/lambda light chain immunoglobulin IVD, antibody

Lambda-PE by Cytognos Sl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Kappa/lambda light chain immunoglobulin IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cytognos Sl

Sources (1)

  • FDA UDI d9e691da-aa32-4b42-8857-7cf22de7648b 35 fields · synced Jun 8, 2026