Sarmix®M2000,100-240V no rotor 90.180.600

GUDID 04038917101974

Sarstedt Aktiengesellschaft & Co.KG

Blood tube mixer IVD Blood tube mixer IVD Blood tube mixer IVD Blood tube mixer IVD Blood tube mixer IVD Blood tube mixer IVD Blood tube mixer IVD Blood tube mixer IVD
Primary Device ID04038917101974
NIH Device Record Key44cce379-86aa-4601-9e71-4ab5b63f7ac8
Commercial Distribution StatusIn Commercial Distribution
Brand NameSarmix®M2000,100-240V no rotor
Version Model Number90.180.600
Catalog Number90.180.600
Company DUNS388000270
Company NameSarstedt Aktiengesellschaft & Co.KG
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
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
GS104038917101974 [Primary]

FDA Product Code

GLEMIXER, BLOOD TUBE

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

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