Primary Device ID | 09348215038939 |
NIH Device Record Key | 8f67dc4f-024f-4c01-a2a4-17b39a23426c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trial Cups |
Version Model Number | 112-152-202 |
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 | 09348215038939 [Primary] |
HWT | Template |
LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
Steralize Prior To Use | true |
Device Is Sterile | false |
[09348215038939]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-06-18 |
Device Publish Date | 2018-10-02 |
09348215038991 | 112-152-578 |
09348215038984 | 112-152-574 |
09348215038977 | 112-152-573 |
09348215038960 | 112-152-205 |
09348215038953 | 112-152-204 |
09348215038946 | 112-152-203 |
09348215038939 | 112-152-202 |
09348215038922 | 112-152-201 |
09348215038915 | 112-152-200 |
09348215038908 | 112-152-199 |
09348215038892 | 112-152-198 |
09348215038885 | 112-152-197 |
09348215038878 | 112-152-196 |
09348215038861 | 112-152-195 |
09348215038854 | 112-152-194 |
09348215038847 | 112-152-193 |
09348215038830 | 112-152-192 |
09348215038823 | 112-152-191 |