Primary Device ID | 00190837142537 |
NIH Device Record Key | 1680ae4e-fd10-4c40-a473-f976c57f5621 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dyna-Link Ti |
Version Model Number | L114-881-1 |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00190837142537 [Primary] |
OVD | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
[00190837142537]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-08 |
Device Publish Date | 2021-06-30 |