Primary Device ID | 09348215067090 |
NIH Device Record Key | 87f5dc30-fc64-4381-b5b2-aed2f5cad835 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aurora Trial Plate 17 |
Version Model Number | 132-16-0110 |
Company DUNS | 751993028 |
Company Name | SIGNATURE ORTHOPAEDICS PTY 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 | 09348215067090 [Primary] |
KWQ | Appliance, Fixation, Spinal Intervertebral Body |
Steralize Prior To Use | true |
Device Is Sterile | false |
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
[09348215067090]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-08 |
Device Publish Date | 2020-06-30 |