Mosaic Ultra™7308U

GUDID 00763000613624

SIZERS 7308U MOSAIC ULTRA AORTIC MDR

MEDTRONIC, INC.

Heart valve annulus sizer, reusable
Primary Device ID00763000613624
NIH Device Record Key02e2d172-c400-4db8-8002-3388a9c2710a
Commercial Distribution StatusIn Commercial Distribution
Brand NameMosaic Ultra™7308U
Version Model Number7308U
Company DUNS006261481
Company NameMEDTRONIC, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
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
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

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100763000613624 [Primary]

FDA Product Code

DTISIZER, HEART-VALVE, PROSTHESIS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


[00763000613624]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-03-11
Device Publish Date2025-03-03

Devices Manufactured by MEDTRONIC, INC.

00199150002184 - NA2026-02-09 COMMUNICATOR TM90D0 DBS US EMAN CABLE
00763000659202 - SimuForm™2026-02-09 RING 7800RR24 SIMUFORM SR 24MM MDR
00763000659219 - SimuForm™2026-02-09 RING 7800RR26 SIMUFORM SR 26MM MDR
00763000659226 - SimuForm™2026-02-09 RING 7800RR28 SIMUFORM SR 28MM MDR
00763000659233 - SimuForm™2026-02-09 RING 7800RR30 SIMUFORM SR 30MM MDR
00763000659240 - SimuForm™2026-02-09 RING 7800RR32 SIMUFORM SR 32MM MDR
00763000659257 - SimuForm™2026-02-09 RING 7800RR34 SIMUFORM SR 34MM MDR
00763000659264 - SimuForm™2026-02-09 RING 7800RR36 SIMUFORM SR 36MM MDR

Trademark Results [Mosaic Ultra]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MOSAIC ULTRA
MOSAIC ULTRA
78470205 3294682 Live/Registered
Medtronic, Inc.
2004-08-19

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