Primary Device ID | 09348215072735 |
NIH Device Record Key | 3063d9b7-99ee-4e91-925d-fa6f65448b6b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lateralised Neutral Trial Liner : SIZE 32/56-58mm |
Version Model Number | 112-15-7256 |
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 | true |
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 | 09348215072735 [Primary] |
LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-01 |
Device Publish Date | 2020-06-23 |
09348215129224 - Verteloc Lumbar Cage | 2024-03-20 |
09348215129231 - Verteloc Lumbar Cage | 2024-03-20 |
09348215129248 - Verteloc Lumbar Cage | 2024-03-20 |
09348215129255 - Verteloc Lumbar Cage | 2024-03-20 |
09348215129262 - Verteloc Lumbar Cage | 2024-03-20 |
09348215129279 - Verteloc Lumbar Cage | 2024-03-20 |
09348215129286 - Verteloc Lumbar Cage | 2024-03-20 |
09348215129293 - Verteloc Lumbar Cage | 2024-03-20 |