Primary Device ID | 09348215038281 |
NIH Device Record Key | 285319ee-3460-4f48-ab14-a76632a37a74 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trial Head |
Version Model Number | 112-182-041 |
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 | 09348215038281 [Primary] |
HWT | Template |
LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
Steralize Prior To Use | true |
Device Is Sterile | false |
[09348215038281]
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 | 2018-10-05 |
09348215038410 | 112-182-046 |
09348215038403 | 112-182-045 |
09348215038397 | 112-182-044 |
09348215038380 | 112-182-043 |
09348215038373 | 112-182-024 |
09348215038366 | 112-182-023 |
09348215038359 | 112-182-022 |
09348215038342 | 112-182-021 |
09348215038335 | 112-182-020 |
09348215038328 | 112-182-019 |
09348215038311 | 112-182-018 |
09348215038304 | 112-182-017 |
09348215038298 | 112-182-042 |
09348215038281 | 112-182-041 |
09348215038274 | 112-182-040 |