GUDID 00673978249933

SHUNT 9046 B-M ASSY REG MED PERIT-90CM

MEDTRONIC PS MEDICAL, INC.

Ventriculoperitoneal shunt
Primary Device ID00673978249933
NIH Device Record Key8b28f099-4ee2-406a-8f3c-7f2a3a2dda50
Commercial Distribution StatusIn Commercial Distribution
Version Model Number9046 B-M
Company DUNS089055867
Company NameMEDTRONIC PS 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 Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Length90 Centimeter
Device Size Text, specify0
Length90 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100673978249933 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JXGShunt, central nervous system and components

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 Date2015-06-29

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