GUDID 00763000306793

CUSTOM PACK CB11A58R SUCTION LN

MEDTRONIC, INC.

Cardiopulmonary bypass system tubing set
Primary Device ID00763000306793
NIH Device Record Key53e1518a-2f85-4843-a0ea-632cf11f839e
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberCB11A58R
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 Kittrue
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
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

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000306793 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DTZOXYGENATOR, CARDIOPULMONARY BYPASS

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-09-27
Device Publish Date2019-09-19

Devices Manufactured by MEDTRONIC, INC.

00199150039371 - NA2025-08-22 CUSTOM PACK BB11U72R1 P/T
00199150040872 - NA2025-08-22 CUSTOM PACK BB4K95R22 HLO PERFNPLEG
00199150041145 - NA2025-08-22 CUSTOM PACK BB12Q87R1 HLN VAMC NASH
00199150041978 - NA2025-08-22 CUSTOM PACK BB10F40R2 ACCESORY
00199150041299 - NA2025-08-19 CUSTOM PACK BB8E60R12 EVL PED E
20199150041118 - NA2025-08-18 CUSTOM PACK BB12E30R1 10PK ACC BRIDGE
20199150041132 - NA2025-08-18 CUSTOM PACK BB5G89R2 2PK T SPRT
00763000876982 - SPRINTER® LEGEND2025-08-18 BALLOON SPL12506X SPR LEG RX US M

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.