LIAISON BRAHMS PCT II GEN

GUDID 08056771103015

DIASORIN SPA

Procalcitonin (PCT) IVD, kit, chemiluminescent immunoassay
Primary Device ID08056771103015
NIH Device Record Keya9a38cf7-9a61-430c-8450-f870901dca04
Commercial Distribution StatusIn Commercial Distribution
Brand NameLIAISON BRAHMS PCT II GEN
Version Model Number318090
Company DUNS630822989
Company NameDIASORIN SPA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com
Phone6514399710
Emailinfo@diasorin.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108056771103015 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2026-02-09
Device Publish Date2018-04-05

Devices Manufactured by DIASORIN SPA

08056771103015 - LIAISON BRAHMS PCT II GEN2026-02-09
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08056771100205 - LIAISON® Control anti-HAV2026-01-19
08056771100571 - LIAISON® Rubella IgG2026-01-19
08056771100588 - LIAISON® Rubella IgG TRI-Controls2026-01-19
08056771100618 - LIAISON® Treponema Assay2026-01-19
08056771101943 - LIAISON® CMV IgM2026-01-15
08056771104029 - LIAISON® Biotrin Parvovirus B19 IgG Plus2024-04-16 Italy manufactured kit.

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