Tube 50ml, 115x28mm, PP 62.559.001

GUDID 04038917189620

Sarstedt Aktiengesellschaft & Co.KG

Assay container IVD, single-use
Primary Device ID04038917189620
NIH Device Record Key0e957aa9-4991-4895-bb5f-baee29ca2b7a
Commercial Distribution StatusIn Commercial Distribution
Brand NameTube 50ml, 115x28mm, PP
Version Model Number62.559.001
Catalog Number62.559.001
Company DUNS388000270
Company NameSarstedt Aktiengesellschaft & Co.KG
Device Count25
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
GS104038917113489 [Primary]
GS104038917189620 [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 Date2022-12-08
Device Publish Date2022-11-30

On-Brand Devices [Tube 50ml, 115x28mm, PP]

0403891716475762.559
0403891718962062.559.001
0403891731431262.559.016
0403891731241762.559.015

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