ITREL® EZ ™

GUDID 00673978933733

PROGRAMMER 7434A ITREL 3 PATIENT

MEDTRONIC, INC.

Active-implantable-device communicator Active-implantable-device communicator Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer Multiple active implantable device programmer
Primary Device ID00673978933733
NIH Device Record Key6069c610-eeef-40f5-98cf-9b36cfab4f0a
Commercial Distribution StatusIn Commercial Distribution
Brand NameITREL® EZ ™
Version Model Number7434A
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 Usefalse
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

Operating and Storage Conditions

Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius
Handling Environment TemperatureBetween -40 Degrees Fahrenheit and 149 Degrees Fahrenheit
Handling Environment TemperatureBetween -40 Degrees Celsius and 65 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100673978933733 [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 Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2014-09-23

Devices Manufactured by MEDTRONIC, INC.

00763000951825 - NA2024-05-31 CUSTOM PACK SSBB12G88R STERILE SMPL
00763000953423 - NA2024-05-31 CUSTOM PACK BB12F51R2 E ASSIST PACK
00763000953614 - NA2024-05-31 CUSTOM PACK HY0A20R46 CHRST NN
00763000953621 - NA2024-05-31 CUSTOM PACK BB11Q49R11 3/8 EC
00763000953638 - NA2024-05-31 CUSTOM PACK BB12A45R1 SMALL LOOP
00763000953645 - NA2024-05-31 CUSTOM PACK BB12A44R2 LRG AV LOOP
20763000953663 - NA2024-05-31 CUSTOM PACK BB12G60R 2PK 2PK CHRST TBL
00763000953676 - NA2024-05-31 CUSTOM PACK BB7B00R26 UW CMAG PK

Trademark Results [ITREL]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ITREL
ITREL
73629635 1446216 Dead/Cancelled
MEDTRONIC, INC.
1986-11-10
ITREL
ITREL
73422274 1313304 Live/Registered
Medtronic, Inc.
1983-04-18
ITREL
ITREL
73184208 1166349 Dead/Cancelled
Medtronic, Inc.
1978-08-31

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.