MPS® Extension Tubing, 6 ft. x 1/8 in. 7001104

GUDID 20634624701148

QUEST MEDICAL INC

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Primary Device ID20634624701148
NIH Device Record Key81edc5d3-5c32-4233-8d08-96539e24f242
Commercial Distribution StatusIn Commercial Distribution
Brand NameMPS® Extension Tubing, 6 ft. x 1/8 in.
Version Model Number7001104
Catalog Number7001104
Company DUNS041810693
Company NameQUEST MEDICAL INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com
Phone800-627-0226
Emailcustserv@questmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100634624701144 [Primary]
GS120634624701148 [Package]
Contains: 00634624701144
Package: Shipper [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DTRHeat-Exchanger, Cardiopulmonary Bypass

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-06-15

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