Albumin BCP (6x20 mL) C22855

GUDID 08058056681973

The Albumin BCP (6x20 mL) assay is an in vitro diagnostic test used for the determination of albumin in human serum or plasma. The assay is intended for professional use only. For In Vitro Diagnostic use only.

SENTINEL CH. SPA

Albumin IVD, reagent
Primary Device ID08058056681973
NIH Device Record Key036eb04a-48c7-4080-be21-297e5e30a10f
Commercial Distribution StatusIn Commercial Distribution
Brand NameAlbumin BCP (6x20 mL)
Version Model NumberC22855
Catalog NumberC22855
Company DUNS429572365
Company NameSENTINEL CH. 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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone9999999999
Emailcustomerservice@sentinel.it

Device Dimensions

Total Volume120 Milliliter

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store between 15 and 30 degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS108058056681973 [Primary]

FDA Product Code

CJWBromcresol Purple Dye-Binding, Albumin

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-03
Device Publish Date2020-02-24

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