Primary Device ID | 05055715612296 |
NIH Device Record Key | fad73ca7-a241-4d82-b106-02144fe12f8e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aorfix AAA Stent Graft Converter with Aorflex Deli |
Version Model Number | SG-HBC-31-A12-22 |
Company DUNS | 775481088 |
Company Name | LOMBARD MEDICAL LIMITED |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 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 | 05055715612296 [Primary] |
MIH | System, Endovascular Graft, Aortic Aneurysm Treatment |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-04-29 |
05055715612296 | Aorfix AAA Stent Graft Converter with Aorflex Delivery System |
05055715612289 | Aorfix AAA Stent Graft Converter with Aorflex Delivery System |
05055715612272 | Aorfix AAA Stent Graft Converter with Aorflex Delivery System |
05055715612265 | Aorfix AAA Stent Graft Converter with Aorflex Delivery System |