Primary Device ID | 20643169938810 |
NIH Device Record Key | 227ce9e1-6561-4bd2-acb5-ab7b093a6dd6 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 9626340 |
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 | 00643169938816 [Primary] |
GS1 | 20643169938810 [Package] Contains: 00643169938816 Package: PK [10 Units] In Commercial Distribution |
IKN | Electromyograph, diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-03-26 |
00763000003036 - NIM Vital™ | 2024-11-15 CONN CABLE NIM4CPB2 PAT INTFC NIM 4.0 |
00763000842543 - Bipolar Stimulating Probe | 2024-11-04 PROBE 8225351 5PK CONCEN BIPO STIM ROHS |
00763000842550 - Bipolar Stimulating Probe | 2024-11-04 PROBE 8225401 5PK SD-SD BIPOL STIM ROHS |
00763000842567 - Bipolar Stimulating Probe | 2024-11-04 PROBE 8225451 5PK PRASS BIPO STIMUL ROHS |
00763000891862 - ENT NIM Electrode | 2024-10-01 PROBE 8225275 BALL TIP 1MM ROHS |
00763000891879 - ENT NIM Electrode | 2024-10-01 PROBE 8225276 BALL TIP 2.3MM ROHS |
00763000580483 - ENT NIM Vital | 2024-09-27 CABLE 1352415 STIM DISSECTION 3M ROHS |
00763000578022 - N/A | 2024-09-24 SPLINT 1528110 25PK EXTERNAL NASAL SMALL |