Primary Device ID | 09348215039752 |
NIH Device Record Key | 2eb35957-c554-436e-927b-f8cfd1985321 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Origin Broach |
Version Model Number | 111-18-1409 |
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 | 09348215039752 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[09348215039752]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-04 |
Device Publish Date | 2018-10-02 |
09348215039783 | 111-18-1809 |
09348215039776 | 111-18-1609 |
09348215039769 | 111-18-1509 |
09348215039752 | 111-18-1409 |
09348215039745 | 111-18-1309 |
09348215039738 | 111-18-1209 |
09348215039721 | 111-18-1109 |
09348215039714 | 111-18-1009 |
09348215039707 | 111-18-0909 |
09348215039691 | 111-18-0809 |
09348215039684 | 111-18-0609 |