GUDID 00643169023314

CABLE 203CX COAXIAL UMBILICAL

MEDTRONIC, INC.

Liquid nitrous oxide coaxial tubing
Primary Device ID00643169023314
NIH Device Record Keyeee0c25d-6ad2-4c7f-a1e8-4d981e27a520
Commercial Distribution StatusIn Commercial Distribution
Version Model Number203CX
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

Operating and Storage Conditions

Handling Environment TemperatureBetween -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
Handling Environment TemperatureBetween -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
Handling Environment TemperatureBetween -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
Handling Environment TemperatureBetween -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
Handling Environment TemperatureBetween -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
Handling Environment TemperatureBetween -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
Handling Environment TemperatureBetween -31 Degrees Fahrenheit and 136 Degrees Fahrenheit
Handling Environment TemperatureBetween -31 Degrees Fahrenheit and 136 Degrees Fahrenheit

Device Identifiers

Device Issuing AgencyDevice ID
GS100643169023314 [Primary]

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 Number3
Public Version Date2018-07-06
Device Publish Date2014-09-23

Devices Manufactured by MEDTRONIC, INC.

00199150042098 - NA2025-09-08 CUSTOM PACK BB8B09R20 HLN OR INFANT
00199150042661 - NA2025-09-08 CUSTOM PACK BB0C01R32 EVL 1/4 SUPPT
00199150042753 - NA2025-09-08 CUSTOM PACK BB9F06R5 EVL WCH NEONA
00199150043392 - NA2025-09-08 CUSTOM PACK BB12D74R5 HLO ALLIDON
00199150043507 - NA2025-09-08 CUSTOM PACK BB12Q89R1 EVL 3/8
00199150043538 - NA2025-09-08 CUSTOM PACK BB12Q60R1 HLO ST BERNAR
00199150044436 - NA2025-09-08 CUSTOM PACK BB9R01R23 HLN OR PEDIA
20199150044454 - NA2025-09-08 CUSTOM PACK BB12R78R 5PK ACC PDEVL

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