Primary Device ID | 09349797000239 |
NIH Device Record Key | 4790efa1-6093-4621-9eeb-65b0dea88457 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | StarPore |
Version Model Number | CI-STARPORE-O |
Catalog Number | CI-STARPORE-O |
Company DUNS | 755739307 |
Company Name | ANATOMICS PTY LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +61395298088 |
contact@anatomics.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 09349797000239 [Primary] |
GWO | Plate, Cranioplasty, Preformed, Alterable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-01-16 |
Device Publish Date | 2020-01-08 |
09349797000239 | StarPore Patient Specific Implant (Other) |
09349797000222 | StarPore Patient Specific Implant (X-Large) |
09349797000215 | StarPore Patient Specific Implant (Large) |
09349797000208 | StarPore Patient Specific Implant (Medium) |
09349797000192 | StarPore Patient Specific Implant (Small) |
09349797002387 | StarPore Patient Specific Implant (SAMPLE) |
09349797001700 | StarPore Patient Specific Implant |
09349797002561 | StarPore Patient Specific Implant (X-Large) |
09349797002554 | StarPore Patient Specific Implant (Large) |
09349797002547 | StarPore Patient Specific Implant (Medium) |
09349797002530 | StarPore Patient Specific Implant (Small) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STARPORE 88418356 not registered Live/Pending |
Scimotana Pty. Ltd. 2019-05-07 |