GUDID 00643169101081

CATH 8598A KIT DISTAL REVISION PF JUNCOS

MEDTRONIC, INC.

General-purpose implantable infusion pump, programmable General-purpose implantable infusion pump, programmable Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit Lumbar cerebrospinal fluid drainage catheterization kit
Primary Device ID00643169101081
NIH Device Record Keyc22da178-835c-40f0-873f-31a8dc79039a
Commercial Distribution StatusIn Commercial Distribution
Version Model Number8598A
Company DUNS796986144
Company NameMEDTRONIC, 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 Producttrue
Single Usetrue
Lot Batchfalse
Serial Numbertrue
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
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
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
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
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
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 Identifiers

Device Issuing AgencyDevice ID
GS100643169101081 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LKKPUMP, INFUSION, IMPLANTED, PROGRAMMABLE

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 Date2016-04-27

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