GUDID 20763000314686

CUSTOM PACK CB9153R5 5PK SUCTION

MEDTRONIC, INC.

Cardiopulmonary bypass system tubing set
Primary Device ID20763000314686
NIH Device Record Key90534e27-760f-4e00-bb41-034aeac1f761
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberCB9153R5
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
GS100763000314675 [Primary]
GS120763000314686 [Package]
Contains: 00763000314675
Package: PK [5 Units]
In Commercial Distribution

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 StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-02-20
Device Publish Date2019-10-07

Devices Manufactured by MEDTRONIC, INC.

00199150071623 - NA2026-03-16 CUSTOM PACK BB11X36R2 EVL SUPPORT
20199150071917 - NA2026-03-16 CUSTOM PACK BB8S03R4 10PK EVL ACCESS
00199150071920 - NA2026-03-16 CUSTOM PACK BB9G55R9 HLO TVA FU
00199150071937 - NA2026-03-16 CUSTOM PACK BB10P43R7 TRIDENT A
00199150071944 - NA2026-03-16 CUSTOM PACK BB12R46R1 EVL TABLE
20199150072020 - NA2026-03-16 CUSTOM PACK BB12T66R 10PK AVL HALI
00199150072033 - NA2026-03-16 CUSTOM PACK BB11W59R9 EVL P-MAG
00199150072040 - NA2026-03-16 CUSTOM PACK BB9E90R12 EVL 3/8 SPRT

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.