tube 10ml, 79x16mm, PP 62.551.201

GUDID 04038917189132

Sarstedt Aktiengesellschaft & Co.KG

Assay container IVD, single-use
Primary Device ID04038917189132
NIH Device Record Key22a9dc99-d7e8-4c57-9de0-76102378fc6d
Commercial Distribution StatusIn Commercial Distribution
Brand Nametube 10ml, 79x16mm, PP
Version Model Number62.551.201
Catalog Number62.551.201
Company DUNS388000270
Company NameSarstedt Aktiengesellschaft & Co.KG
Device Count100
DM Exemptfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS104038917112901 [Primary]
GS104038917189132 [Unit of Use]

FDA Product Code

KDTCONTAINER, SPECIMEN MAILER AND STORAGE, STERILE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-07-31
Device Publish Date2023-07-22

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