Primary Device ID | 00763000172893 |
NIH Device Record Key | d034d0c5-e769-417a-af36-8b43c5878cbb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Indigo |
Version Model Number | 1845020-R |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
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 | |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00763000172893 [Primary] |
HAB | SAW, POWERED, AND ACCESSORIES |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00763000172893]
Ethylene Oxide;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-11-22 |
Device Publish Date | 2018-09-29 |
00763000172893 | ATT 1845020-R INDIGO OTOL ANGLED REFURB |
00763000172886 | ATT 1845010-R INDIGO OTOL STRAIGHT RFURB |
00763000172879 | ATT 1845020 INDIGO OTOL ANGLED |
00763000172862 | ATT 1845010 INDIGO OTOL STRAIGHT |
00763000299217 | INSTRUMENT TRAY 1845040 INDIGO |