Primary Device ID | 00190837105198 |
NIH Device Record Key | ccf415b6-331d-484f-b6ab-5aa42938d3c4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProLift Lateral |
Version Model Number | 151-1092 |
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 | 00190837105198 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
[00190837105198]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-19 |
Device Publish Date | 2021-10-11 |