GUDID 00763000140120

BLADE 9564046 1/4 TUBE S 60MM TI

MEDTRONIC SOFAMOR DANEK, INC.

Surgical retraction system, reusable
Primary Device ID00763000140120
NIH Device Record Keya3d4dbcc-e54a-46b0-8e04-4d3788de0356
Commercial Distribution StatusIn Commercial Distribution
Version Model Number9564046
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
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

Device Dimensions

Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter
Length60 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000140120 [Primary]

FDA Product Code

GADRETRACTOR

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


[00763000140120]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-10-04
Device Publish Date2021-09-24

Devices Manufactured by MEDTRONIC SOFAMOR DANEK, INC.

00199150021543 - Medtronic Reusable Instruments2025-07-21 HOLDER X0625020 BONE GRAFT
00199150021550 - Medtronic Reusable Instruments2025-07-21 SLAP HAMMER X0625025 BONE GRAFT HOLDER
00763000703578 - Medtronic Reusable Instruments2025-07-21 CAM SPREADER TRIAL 4000017 6 DEG 17MM
00763000703592 - Medtronic Reusable Instruments2025-07-21 CAM SPREADER TRIAL 4010010 12 DEG 10MM
00763000703608 - Medtronic Reusable Instruments2025-07-21 CAM SPREADER TRIAL 4010011 12 DEG 11MM
00763000703615 - Medtronic Reusable Instruments2025-07-21 CAM SPREADER TRIAL 4010012 12 DEG 12MM
00763000703622 - Medtronic Reusable Instruments2025-07-21 CAM SPREADER TRIAL 4010013 12 DEG 13MM
00763000703639 - Medtronic Reusable Instruments2025-07-21 CAM SPREADER TRIAL 4010014 12 DEG 14MM

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