Primary Device ID | 00643169789555 |
NIH Device Record Key | 0999de87-e2fb-4d4d-9c46-64bbfb9926bc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NIM CONTACT® |
Version Model Number | 8229506 |
Company DUNS | 835465063 |
Company Name | MEDTRONIC XOMED, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
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 | 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 |
Outer Diameter | 9 Millimeter |
Outer Diameter | 9 Millimeter |
Outer Diameter | 9 Millimeter |
Outer Diameter | 9 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169789555 [Primary] |
ETN | STIMULATOR, NERVE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-11-06 |
00643169789579 | EMG TUBE 8229508 NIM CONT 8MM ROHS |
00643169789562 | EMG TUBE 8229507 NIM CONT 7MM ROHS |
00643169789555 | EMG TUBE 8229506 NIM CONT 6MM ROHS |
00643169358775 | ENDOTRACH TUBE 8229508 CONT EMG 8MM ROHS |
00643169358768 | ENDOTRACH TUBE 8229507 CONT EMG 7MM ROHS |
00643169358751 | ENDOTRACH TUBE 8229506 CONT EMG 6MM ROHS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NIM CONTACT 78600100 3276757 Live/Registered |
Medtronic Xomed, Inc. 2005-04-01 |