Primary Device ID | 00190837175238 |
NIH Device Record Key | 1965e84a-a549-4dab-ad8e-53909471c32f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ARx SAI |
Version Model Number | 18-85100-09 |
Company DUNS | 183641617 |
Company Name | Life Spine, 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190837175238 [Primary] |
NKB | Thoracolumbosacral Pedicle Screw System |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00190837175238]
Moist Heat or Steam Sterilization
[00190837175238]
Moist Heat or Steam Sterilization
[00190837175238]
Moist Heat or Steam Sterilization
[00190837175238]
Moist Heat or Steam Sterilization
[00190837175238]
Moist Heat or Steam Sterilization
[00190837175238]
Moist Heat or Steam Sterilization
[00190837175238]
Moist Heat or Steam Sterilization
[00190837175238]
Moist Heat or Steam Sterilization
[00190837175238]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-12 |
Device Publish Date | 2024-12-04 |
00190837175382 | 18-9570-09 |
00190837175238 | 18-85100-09 |
00190837175191 | 18-8580-09 |
00190837175177 | 18-8570-09 |
00190837175214 | 18-8590-09 |