GUDID 00613994721907

LEAD 3777-45 OCTAD 1X8 LZ 6MM SP EN eMAN

MEDTRONIC, INC.

Neural-tissue electrical stimulation lead
Primary Device ID00613994721907
NIH Device Record Key08c09487-0a26-4fce-9461-85891bb411c7
Commercial Distribution StatusIn Commercial Distribution
Version Model Number3777-45
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 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

Device Dimensions

Length45 Centimeter
Length45 Centimeter
Length45 Centimeter

Operating and Storage Conditions

Storage Environment TemperatureBetween -30 Degrees Fahrenheit and 135 Degrees Fahrenheit
Storage Environment TemperatureBetween -30 Degrees Fahrenheit and 135 Degrees Fahrenheit
Storage Environment TemperatureBetween -30 Degrees Fahrenheit and 135 Degrees Fahrenheit
Storage Environment TemperatureBetween -30 Degrees Fahrenheit and 135 Degrees Fahrenheit
Storage Environment TemperatureBetween -34 Degrees Celsius and 57 Degrees Celsius
Storage Environment TemperatureBetween -30 Degrees Fahrenheit and 135 Degrees Fahrenheit

Device Identifiers

Device Issuing AgencyDevice ID
GS100613994721907 [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 Number3
Public Version Date2018-07-06
Device Publish Date2014-09-23

Devices Manufactured by MEDTRONIC, INC.

00763000613617 - Mosaic™7308C2025-03-11 SIZERS 7308C MOSAIC CINCH AORTIC MDR
00763000613624 - Mosaic Ultra™7308U2025-03-11 SIZERS 7308U MOSAIC ULTRA AORTIC MDR
00763000613631 - Mosaic™73102025-03-11 OBTURATORS 7310 MOSAIC MITRAL MDR
00763000613648 - NA2025-03-11 HANDLE 7639 VALVE MDR
00763000613655 - NA2025-03-11 HANDLE 7639XL VALVE XL MDR
00763000613662 - NA2025-03-11 ACCESSORY 7642 LOCK NUT MDR
00763000614034 - Hancock™ II 75052025-03-11 OBTURATOR 7505SET HK II AORTIC MDR
00763000614041 - Hancock™ II 75102025-03-11 OBTURATOR 7510SET HK II MITRAL MDR

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.