Primary Device ID | 07290115935431 |
NIH Device Record Key | ea03a066-f623-4d04-ab65-8c8c22488ba8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Rod Pusher |
Version Model Number | 83203 |
Company DUNS | 649220779 |
Company Name | PREMIA SPINE LTD |
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 | 07290115935431 [Primary] |
NKB | Thoracolumbosacral Pedicle Screw System |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
[07290115935431]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-09 |
Device Publish Date | 2024-10-01 |
07290115935509 | 86604 |
07290115935431 | 83203 |