GUDID 00885074200330

ACCY KIT 355032 NDLE TOUHY 14GA 3.5IN ID

MEDTRONIC, INC.

Neurosurgical procedure kit, non-medicated, single-use
Primary Device ID00885074200330
NIH Device Record Keyc59f51e9-b06c-4bd9-a826-77294759dcd8
Commercial Distribution Discontinuation2018-08-13
Commercial Distribution StatusNot in Commercial Distribution
Version Model Number355032
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100885074200330 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LGWSTIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-10-02
Device Publish Date2014-09-23

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00199150001880 - IN.PACT™ 0182026-03-27 DCB 018XL IPU05020020P D5.0 L200 UL0200
00199150001903 - IN.PACT™ 0182026-03-27 DCB 018XL IPU05025013P D5.0 L250 UL0130
00199150001910 - IN.PACT™ 0182026-03-27 DCB 018XL IPU05025020P D5.0 L250 UL0200

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