GUDID 00643169887435

ACCY KIT 3550-03 DBS TWSTLCK SCRNCBL FWU

MEDTRONIC, INC.

Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use Neurosurgical procedure kit, non-medicated, single-use
Primary Device ID00643169887435
NIH Device Record Key0533f68e-c572-4716-b5d5-d0b78c7d611c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number3550-03
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
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
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169887435 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHLSTIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS

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 Date2017-10-08

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