CATH 8578 SC CONN UPDATE PROX REV JUNCOS Medical Device Identification

GUDID 00643169158108

CATH 8578 SC CONN UPDATE PROX REV JUNCOS

MEDTRONIC, INC.

Spinal infusion/drainage catheter Spinal infusion/drainage catheter 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 ID	00643169158108
NIH Device Record Key	e0ef9f03-1155-402f-b3bb-4ac505c5eb94
Commercial Distribution Status	In Commercial Distribution
Version Model Number	8578
Company DUNS	796986144
Company Name	MEDTRONIC, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	true
Single Use	true
Lot Batch	false
Serial Number	true
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169158108 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Approval: P860004

FDA Product Code

LKK	PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	3
Public Version Date	2018-07-06
Device Publish Date	2016-04-27

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