Primary Device ID | 20681490176709 |
NIH Device Record Key | 80e11398-cf5f-4bc7-900e-287f973bd995 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 8225103 |
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 | 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 | 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 | 00681490176705 [Primary] |
GS1 | 20681490176709 [Package] Contains: 00681490176705 Package: PK [5 Units] In Commercial Distribution |
ETN | STIMULATOR, NERVE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-04-17 |
00763000849573 - PTEYE Parathyroid Detection System | 2024-04-12 CONSOLE PTEYE |
00763000849580 - PTEYE Parathyroid Detection System | 2024-04-12 CONSOLE PTEYE-RF REFURBISHED |
00763000882389 - NIM | 2024-02-12 EMG TUBE 8229306 NIM STD 6MM ROHS |
00763000882396 - NIM | 2024-02-12 EMG TUBE 8229307 NIM STD 7MM ROHS |
00763000882402 - NIM | 2024-02-12 EMG TUBE 8229308 NIM STD 8MM ROHS |
00763000882419 - NIM | 2024-02-12 EMG TUBE 8229506 NIM CONT 6MM ROHS |
00763000882426 - NIM | 2024-02-12 EMG TUBE 8229507 NIM CONT 7MM ROHS |
00763000882433 - NIM | 2024-02-12 EMG TUBE 8229508 NIM CONT 8MM ROHS |