Primary Device ID | 00763000318383 |
NIH Device Record Key | cbb4c713-9f23-4807-aa18-4c4d93d1a5a6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MOSAIC™ |
Version Model Number | 7308C |
Company DUNS | 079527232 |
Company Name | MEDTRONIC 3F THERAPEUTICS, 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 | |
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 | |
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 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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000318383 [Primary] |
DTI | SIZER, HEART-VALVE, PROSTHESIS |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
[00763000318383]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-19 |
Device Publish Date | 2024-08-11 |
00763000318390 | OBTURATORS 7310 MOSAIC MITRAL 26L CE |
00763000318383 | SIZERS 7308C MOSAIC AORTIC 26L CE |