Primary Device ID | 00643169553019 |
NIH Device Record Key | 6465973e-0a1c-440f-83b0-e946e6e817ca |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | XPS® |
Version Model Number | 1898200TLO |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | true |
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 | false |
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 | 00643169553019 [Primary] |
ERL | DRILL, SURGICAL, ENT (ELECTRIC OR PNEUMATIC) INCLUDING HANDPIECE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
[00643169553019]
Ethylene Oxide;Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-22 |
Device Publish Date | 2016-05-01 |
00613994598301 | MICRODEBRIDER 1898200TRF IGS M4 REFURB |
00643169882836 | MICRODEBRIDER 1898200TLO LOANER M4 IGS |
00643169882799 | MICRODEBRIDER 1898200TRF IGS M4 REFURB |
00643169882706 | MICRODEBRIDER 1898200T IGS M4 ROHS |
00643169553019 | MICRODEBRIDER 1898200TLO LOANER M4 IGS |
00643169360846 | HANDPIECE 1897200 MAGNUM II EN ROHS |
00643169350663 | CONSOLE 1894440 MICRO MICRODEBRIDER ROHS |
00681490048941 | FOOTSWITCH 1895410 XPS SINGLE FUNCTION |
00681490048880 | FOOTSWITCH 1895400 XPS |