GUDID 00763000241568

CUSTOM PACK HY8L14R6 HYBRID

MEDTRONIC, INC.

Cardiopulmonary bypass system tubing set
Primary Device ID00763000241568
NIH Device Record Key4e968658-f260-4dd8-a2ae-70a80f1b5d4d
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberHY8L14R6
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
GS100763000241568 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWFCatheter, cannula and tubing, vascular, cardiopulmonary bypass

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-03-11
Device Publish Date2019-02-07

Devices Manufactured by MEDTRONIC, INC.

00199150029815 - NA2025-07-18 CUSTOM PACK BB9J91R11 CP PRIME
00199150029839 - NA2025-07-18 CUSTOM PACK BB12B96R7 1/4 SPECTRUM
00199150031603 - NA2025-07-18 CUSTOM PACK BB2R88R9 PUMP/TABL
00199150032457 - NA2025-07-18 CUSTOM PACK BB8L48R9 TABLE PK
00199150033430 - NA2025-07-18 CUSTOM PACK BB12E24R9 UNC GOLD PD
00199150033461 - NA2025-07-18 CUSTOM PACK BB12Q81R H/L 1/2 IN TU
00199150033546 - NA2025-07-18 CUSTOM PACK BB5N65R17 OSU E
00199150033553 - NA2025-07-18 CUSTOM PACK BB12Q62R NORTON HEALTH

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