Sample Diluent

GUDID 06925912716709

Sample Diluent I, 45 mL×2 bottles

Shenzhen YHLO Biotech Co., Ltd.

Buffered sample diluent IVD, automated/semi-automated system
Primary Device ID06925912716709
NIH Device Record Keya4bdffae-5817-44e6-9dd0-8ab376eff569
Commercial Distribution StatusIn Commercial Distribution
Brand NameSample Diluent
Version Model NumberC89919
Company DUNS420735989
Company NameShenzhen YHLO Biotech Co., Ltd.
Device Count2
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106925912716693 [Primary]
GS106925912716709 [Unit of Use]

FDA Product Code

PPMGeneral Purpose Reagent

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-03
Device Publish Date2022-10-26

On-Brand Devices [Sample Diluent]

06925912716785Sample Diluent I-1, 0.57 mL×100 PCS
06925912716709Sample Diluent I, 45 mL×2 bottles
06925912716686Sample Diluent H, 45 mL×2 bottles
06925912716655Sample Diluent G, 45 mL×2 bottles
06925912716662Sample Diluent D, 45 mL×2 bottles
06925912716778Sample Diluent D, 120 microliter x100 PCS
06925912716617Sample Diluent B, 45 mL×2 bottles
06925912716594Sample Diluent A, 45 mL×2 bottles

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