GUDID 20613994775560

CABLE 203CXC COAXIAL UMBILICAL BOX 12

MEDTRONIC, INC.

Liquid nitrous oxide coaxial tubing
Primary Device ID20613994775560
NIH Device Record Keye60ee219-2b5b-4a55-818c-1375cefbbb0b
Commercial Distribution Discontinuation2018-09-05
Commercial Distribution StatusNot in Commercial Distribution
Version Model Number203CXC
Company DUNS006261481
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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS100613994775566 [Primary]
GS120613994775560 [Package]
Contains: 00613994775566
Package: PK [12 Units]
Discontinued: 2018-09-05
Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPBCardiac ablation percutaneous catheter

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-10-05
Device Publish Date2014-09-23

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