N/A

GUDID 00763000571092

ACCY 3755-40 TUNNELNG TOOL DBS EMAN LL61

Covidien LP

Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use Subcutaneous tunneller, single-use
Primary Device ID00763000571092
NIH Device Record Keyf8dfeca3-238f-4328-a73c-7a0c178910a9
Commercial Distribution StatusIn Commercial Distribution
Brand NameN/A
Version Model Number3755-40
Company DUNS058614483
Company NameCovidien LP
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
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
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

Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter
Length40 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000571092 [Primary]

FDA Product Code

HAOINSTRUMENT, SURGICAL, NON-POWERED

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-06-13
Device Publish Date2022-06-04

On-Brand Devices [N/A]

00821684074176ATHERECTOMY FG02550 CUTTERDRIVER V04
00763000571092ACCY 3755-40 TUNNELNG TOOL DBS EMAN LL61

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