Reuter Venturi™

GUDID 20763000039770

VENT TUBE 1070031 5PK VENTURI BOBB 1.27

MEDTRONIC XOMED, INC.

Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube Tympanostomy tube
Primary Device ID20763000039770
NIH Device Record Key7d7d7a60-0d10-4626-917d-062c2bdc3f2a
Commercial Distribution StatusIn Commercial Distribution
Brand NameReuter Venturi™
Version Model Number1070031
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

Device Dimensions

Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter
Lumen/Inner Diameter1.27 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000039776 [Primary]
GS120763000039770 [Package]
Contains: 00763000039776
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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-19
Device Publish Date2020-05-11

On-Brand Devices [Reuter Venturi™]

20681490032791VENT TUBE 1070032 10PK BOBBIN PAIR 1.27
20681490032777VENT TUBE 1070031 5PK VENTURI BOBB 1.27
20681490032746VENT TUBE 1070011 5PK VENTURI BOBB 1.02
20763000039787VENT TUBE 1070032 10PK BOBBIN PAIR 1.27
20763000039770VENT TUBE 1070031 5PK VENTURI BOBB 1.27

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