Primary Device ID | 00643169913004 |
NIH Device Record Key | 9518e4a1-4451-45a8-953a-80a874351371 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 9735733 |
Company DUNS | 835233107 |
Company Name | MEDTRONIC NAVIGATION, 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 | 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 |
Lumen/Inner Diameter | 3.2 Millimeter |
Lumen/Inner Diameter | 3.2 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00643169913004 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00643169913004]
Moist Heat or Steam Sterilization
[00643169913004]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-02-11 |
00763000927127 - Medtronic | 2024-12-13 INST SET 9735283 SOLERA 5.5/6.0 DRVR |
00763000927189 - Medtronic | 2024-12-13 INST SET 9734495 REFERENCING STD |
00763000927233 - Medtronic | 2024-12-13 INST SET 9734494 TACTILE PROBES |
00763000922412 - Medtronic | 2024-11-25 INST SET 9733935 CRANIAL PASSIVE |
00763000927035 - NavLock™ | 2024-11-25 INST SET 9734833 UNIVERSAL NAVLOCK |
00763000927042 - NavLock™ | 2024-11-25 INST SET 9734834 CAPSTONE TRIALS |
00763000927059 - NavLock™ | 2024-11-25 INST SET 9734835 CLYDESDALE TRIALS |
00763000927066 - Medtronic | 2024-11-25 INST SET 9734836 TLIF/DLIF INSERTER |