Push cap, neutral 65.723

GUDID 04038917165921

Sarstedt Aktiengesellschaft & Co.KG

Test tube/reservoir cap IVD
Primary Device ID04038917165921
NIH Device Record Key0eee2ea7-23fd-4597-9302-9fcc88fcfc77
Commercial Distribution StatusIn Commercial Distribution
Brand NamePush cap, neutral
Version Model Number65.723
Catalog Number65.723
Company DUNS388000270
Company NameSarstedt Aktiengesellschaft & Co.KG
Device Count1000
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
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

Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com
Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com
Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com
Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com
Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com
Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com
Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com
Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104038917083713 [Primary]
GS104038917165921 [Unit of Use]

FDA Product Code

NNKCONTAINER, SPECIMEN MAILER AND STORAGE, NON-STERILE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-12-08
Device Publish Date2022-11-30

On-Brand Devices [Push cap, neutral]

0403891752418665.793.030
0403891716626365.782
0403891716592165.723
0403891716571665.697
0403891716327965.109

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