Archiving Cap with filter 65.647.025

GUDID 04038917268226

Sarstedt Aktiengesellschaft & Co.KG

Test tube/reservoir cap
Primary Device ID04038917268226
NIH Device Record Keyd363e8e9-24b8-482a-8543-befddd752329
Commercial Distribution StatusIn Commercial Distribution
Brand NameArchiving Cap with filter
Version Model Number65.647.025
Catalog Number65.647.025
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
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
Phone+1(800)257-5101
Emailcustomerservice.us@sarstedt.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104038917268219 [Primary]
GS104038917268226 [Unit of Use]

FDA Product Code

LXGEQUIPMENT, LABORATORY, GENERAL PURPOSE, LABELED OR PROMOTED FOR A SPECIFIC MEDICAL USE

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-02-17
Device Publish Date2023-02-09

On-Brand Devices [Archiving Cap with filter]

0403891725009265.647.020
0403891726822665.647.025
04038917988292Archiving Cap with filter

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