Primary Device ID | 00643169309593 |
NIH Device Record Key | bf3fe70c-ec70-4e64-a9c7-ea49a94ea151 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AxiEM™ Spine Reference Clamp |
Version Model Number | 9735164 |
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 | true |
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 | |
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 | 00643169309593 [Primary] |
HAW | Neurological stereotaxic Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
[00643169309593]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-06-05 |
00613994233738 | CLAMP 9733037 AXIEM SPINE REFERENCE |
00643169309593 | INST KIT 9735164 LIGHT REF CLAMP |
00763000223045 | CLAMP 9733037 AXIEM SPINE REFERENCE |
00763000210427 | INST KIT 9735164 LIGHT REF CLAMP |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AXIEM 77453029 3880346 Live/Registered |
NATIONAL INSTRUMENTS CORPORATION 2008-04-20 |
AXIEM 77453025 3818944 Live/Registered |
NATIONAL INSTRUMENTS CORPORATION 2008-04-20 |
AXIEM 77228512 not registered Dead/Abandoned |
Applied Wave Research, Inc. 2007-07-12 |
AXIEM 77228487 not registered Dead/Abandoned |
Applied Wave Research, Inc. 2007-07-12 |