Primary Device ID | 07290115934830 |
NIH Device Record Key | 8f64982f-3361-4cf6-98f4-2a437e7e2c23 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Feeler Gauge - Thin |
Version Model Number | 87352 |
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 | 07290115934830 [Primary] |
NKB | Thoracolumbosacral Pedicle Screw System |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
Moist Heat or Steam Sterilization
[07290115934830]
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 |