Primary Device ID | 08053175004382 |
NIH Device Record Key | feb07a44-08b2-480f-b07f-e9115829f464 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cement Injection Cannula |
Version Model Number | 495041420 |
Company DUNS | 437941789 |
Company Name | ADRIA SRL |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08053175004382 [Primary] |
OAR | Injector, Vertebroplasty (Does Not Contain Cement) |
Steralize Prior To Use | true |
Device Is Sterile | true |
[08053175004382]
Ethylene Oxide
[08053175004382]
Ethylene Oxide
[08053175004382]
Ethylene Oxide
[08053175004382]
Ethylene Oxide
[08053175004382]
Ethylene Oxide
[08053175004382]
Ethylene Oxide
[08053175004382]
Ethylene Oxide
[08053175004382]
Ethylene Oxide
[08053175004382]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-04-15 |
Device Publish Date | 2025-04-07 |
08033737113790 - HERNIATOME | 2025-04-15 Percutaneous Discectomy Device |
08033737119983 - HERNIATOME | 2025-04-15 Percutaneous Discectomy Device |
08053175003439 - Vertebroplasty Injector Kit | 2025-04-15 Vertebroplasty Set |
08053175004238 - Hollow Drill | 2025-04-15 DRILL |
08053175004382 - Cement Injection Cannula | 2025-04-15Cement injection cannula |
08053175004382 - Cement Injection Cannula | 2025-04-15 Cement injection cannula |
08053175016125 - Vertebroplasty Needle | 2025-04-15 |
08033737117538 - Trocar | 2024-08-21 |
08033737117545 - Trocar | 2024-08-21 |