LIAISON Q.S.E.T. Buffer

GUDID 08056771602617

Diasorin Inc.

Clinical specimen extraction buffer IVD
Primary Device ID08056771602617
NIH Device Record Keyc8c30887-e59a-49ac-9413-ece356807728
Commercial Distribution StatusIn Commercial Distribution
Brand NameLIAISON Q.S.E.T. Buffer
Version Model Number319135
Company DUNS033429783
Company NameDiasorin Inc.
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone651-439-9710
Emailinfo@diasorin.com
Phone651-439-9710
Emailinfo@diasorin.com
Phone651-439-9710
Emailinfo@diasorin.com
Phone651-439-9710
Emailinfo@diasorin.com
Phone651-439-9710
Emailinfo@diasorin.com
Phone651-439-9710
Emailinfo@diasorin.com
Phone651-439-9710
Emailinfo@diasorin.com
Phone651-439-9710
Emailinfo@diasorin.com
Phone651-439-9710
Emailinfo@diasorin.com

Device Identifiers

Device Issuing AgencyDevice ID
GS108056771602617 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-11-06
Device Publish Date2019-02-19

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