Medtronic Transportation/Sterilization Cassettes

GUDID 00721902957123

CASE 7059532L LEG STND HK MOD LID TI

MEDTRONIC SOFAMOR DANEK, INC.

Instrument tray
Primary Device ID00721902957123
NIH Device Record Key9058a114-1600-4317-ad70-9eda3fb85066
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedtronic Transportation/Sterilization Cassettes
Version Model Number7059532L
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, 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 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
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
GS100721902957123 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTCBath, sitz, nonpowered

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


[00721902957123]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-08-09
Device Publish Date2019-02-04

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00763000889470 - ATLANTIS® Anterior Cervical Plate System2025-06-24 SCREW 3125513 4.5 X 13 SELF DRILL VAR
00763000873608 - DIVERGENCE™ ANTERIOR CERVICAL FUSION SYSTEM2025-06-24 SCREW PK2 G7733513 MINIP S-D 3.5MM X13MM
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