← Back to catalogue

PE-Conjugated Streptavidin

FDA UDI

Class U (US FDA UDI)

by One Lambda, Inc.

Identity

Trade Name
PE-Conjugated Streptavidin FDA UDI
Generic Name
HLA class I & II antigen tissue typing IVD, kit, multiplex FDA UDI
Device Name
For use in the detection of biotinylated proteins and nucleic acids in biotinylated proteins and nucleic acids in LABType™ SSO TYPING TESTS and LABType XR and CWD DNA Typing Test assays. FDA UDI
Model / Reference
N/A FDA UDI
Description
For use in the detection of biotinylated proteins and nucleic acids in biotinylated proteins and nucleic acids in LABType™ SSO TYPING TESTS and LABType XR and CWD DNA Typing Test assays. FDA UDI

Identifiers

Catalog Number
LSPSAB2 FDA UDI
Primary DI / UDI-DI
00812117015484 FDA UDI
FDA Product Code
MZI FDA UDI
GMDN Term
HLA class I & II antigen tissue typing IVD, kit, multiplex FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Category: HLA class I & II antigen tissue typing IVD, kit, multiplex

PE-Conjugated Streptavidin by One Lambda, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as HLA class I & II antigen tissue typing IVD, kit, multiplex.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
One Lambda, Inc.

Sources (1)

  • FDA UDI c255879a-5886-4e96-80db-145d24b069a6 36 fields · synced May 30, 2026