Primary Device ID | 08800015909495 |
NIH Device Record Key | 2b8d60f9-d4d0-42d3-95bd-5416668052e5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ANAX™ OCT SPINAL SYSTEM |
Version Model Number | OSA4546 |
Company DUNS | 688811082 |
Company Name | U&I CORPORATION |
Device Count | 1 |
DM Exempt | true |
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 | true |
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 |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a cool dry place. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08800015909495 [Primary] |
NKG | Orthosis, cervical pedicle screw spinal fixation |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
[08800015909495]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-06-17 |
Device Publish Date | 2016-11-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ANAX 97056657 not registered Live/Pending |
Anaxdent North America LLC 2021-10-01 |
![]() ANAX 88571862 not registered Live/Pending |
Corbett & Brown Inc. 2019-08-08 |
![]() ANAX 87276522 5237188 Live/Registered |
Microtech Knives, Inc. 2016-12-21 |
![]() ANAX 86459418 4772772 Live/Registered |
ANAX Business Technologies, LLC 2014-11-19 |
![]() ANAX 79024628 3275432 Dead/Cancelled |
DOMAINE GEROVASSILIOU S.A. 2006-05-22 |
![]() ANAX 77205255 not registered Dead/Abandoned |
Archon Capital Management LLC 2007-06-13 |