Pope Activent®

GUDID 20681490030780

VENT TUBE 1035004 ACTIVENT 5PK POPE GROM

MEDTRONIC XOMED, INC.

Tympanostomy tube
Primary Device ID20681490030780
NIH Device Record Keyeb90da17-a45b-4a08-8a9b-f092af49f622
Commercial Distribution StatusIn Commercial Distribution
Brand NamePope Activent®
Version Model Number1035004
Company DUNS835465063
Company NameMEDTRONIC XOMED, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
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
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
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
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
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100681490030786 [Primary]
GS120681490030780 [Package]
Contains: 00681490030786
Package: PK [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ETDTUBE, TYMPANOSTOMY

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 Date2015-07-13

Devices Manufactured by MEDTRONIC XOMED, INC.

00763000309480 - Causse/Polycel2025-07-01 PROSTHESIS 1156376 CAUSSE FLPL PARTIAL
20763000870359 - Microgel2025-07-01 VENT TUBE 1082201 5PK PAPA TYPE 1.14
20763000870366 - Sheehy2025-07-01 VENT TUBE 1083301 5PK SHEEHY TYPE 1.27
20763000870373 - 207630008703732025-07-01 VENT TUBE 1084401 5PK GROMMET 1.27
20763000870380 - Reuter2025-07-01 VENT TUBE 1010201 5PK BOBBIN 1.14 FLPL
20763000870403 - Sheehy2025-07-01 VENT TUBE 1013301 5PK BUTTON 1.27 FLPL
20763000870410 - Donaldson2025-07-01 VENT TUBE 1015101 5PK DONLDSN 1.14 FLPL
20763000870427 - Shepard2025-07-01 VENT TUBE 1016101 5PK GROMMET 1.14 FLPL

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