Primary Device ID | 00763000613624 |
NIH Device Record Key | 02e2d172-c400-4db8-8002-3388a9c2710a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mosaic Ultra™7308U |
Version Model Number | 7308U |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000613624 [Primary] |
DTI | SIZER, HEART-VALVE, PROSTHESIS |
Steralize Prior To Use | true |
Device Is Sterile | false |
[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
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-11 |
Device Publish Date | 2025-03-03 |
00763000613617 - Mosaic™7308C | 2025-03-11 SIZERS 7308C MOSAIC CINCH AORTIC MDR |
00763000613624 - Mosaic Ultra™7308U | 2025-03-11SIZERS 7308U MOSAIC ULTRA AORTIC MDR |
00763000613624 - Mosaic Ultra™7308U | 2025-03-11 SIZERS 7308U MOSAIC ULTRA AORTIC MDR |
00763000613631 - Mosaic™7310 | 2025-03-11 OBTURATORS 7310 MOSAIC MITRAL MDR |
00763000613648 - NA | 2025-03-11 HANDLE 7639 VALVE MDR |
00763000613655 - NA | 2025-03-11 HANDLE 7639XL VALVE XL MDR |
00763000613662 - NA | 2025-03-11 ACCESSORY 7642 LOCK NUT MDR |
00763000614034 - Hancock™ II 7505 | 2025-03-11 OBTURATOR 7505SET HK II AORTIC MDR |
00763000614041 - Hancock™ II 7510 | 2025-03-11 OBTURATOR 7510SET HK II MITRAL MDR |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MOSAIC ULTRA 78470205 3294682 Live/Registered |
Medtronic, Inc. 2004-08-19 |