GUDID 20721902844342

CANNULA KIT DLP2X28R 5PK DR SETSER

MEDTRONIC, INC.

Cardiopulmonary bypass system tubing set
Primary Device ID20721902844342
NIH Device Record Key743f48e6-3e18-43eb-96d5-1a294754c7f4
Commercial Distribution Discontinuation2017-08-25
Commercial Distribution StatusNot in Commercial Distribution
Version Model NumberDLP2X28R
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 Perscriptionfalse
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
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100721902844348 [Primary]
GS120721902844342 [Package]
Contains: 00721902844348
Package: PK [5 Units]
Discontinued: 2017-08-25
Not in Commercial Distribution

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 StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-05-22

Devices Manufactured by MEDTRONIC, INC.

00763000763152 - NA2025-10-07 SW APP P7A2C11 ALTAVIVA CLINICIAN
00763000763817 - NA2025-10-07 SW APP P7A2P11 ALTAVIVA PATIENT
00763000929367 - Altaviva™2025-10-07 KIT P7K2C001 ALTAVIVA CLINICIAN
00763000935627 - Altaviva™2025-10-07 KIT P7K2P001 ALTAVIVA PATIENTA^
00763000936433 - Altaviva™2025-10-07 INS P7850N ALTAVIVA NEUROSTIMULATOR RC
00763000936440 - NA2025-10-07 ACCESSORY P71001 POCKET DISSECTOR
00199150050161 - NA2025-09-29 CUSTOM PACK HLO BB12D44R4 PUMP PK
00199150050178 - NA2025-09-29 CUSTOM PACK BB4W67R26 EVL ADULT E

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