Primary Device ID | 00850040139952 |
NIH Device Record Key | 95d49744-c797-4449-9987-c7a581464a5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lateral Removal Tool |
Version Model Number | SR21-6007 |
Company DUNS | 004095409 |
Company Name | SURGENTEC, LLC |
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 | true |
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 | 00850040139952 [Primary] |
OUR | Sacroiliac Joint Fixation |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
[00850040139952]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-11 |
Device Publish Date | 2024-11-01 |