Primary Device ID | 00811806010663 |
NIH Device Record Key | 7071dbb9-4fd5-4861-b48c-1c07ee0b9d28 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AMPLATZER™ |
Version Model Number | TorqVue™ 45 |
Catalog Number | 9-EITV12F45/80 |
Company DUNS | 966215829 |
Company Name | AGA MEDICAL CORPORATION |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com | |
Phone | +1(855)478-5833 |
customerservice@sjm.com |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Catheter Gauge | 12 French |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN A DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN A DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Special Storage Condition, Specify | Between 0 and 0 *STORE IN DRY PLACE. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00811806010663 [Primary] |
DQY | CATHETER, PERCUTANEOUS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-03-09 |
00811806014111 | Delivery Sheath |
00811806012551 | Delivery Sheath |
00811806012513 | Delivery Sheath |
00811806012476 | Delivery Sheath |
00811806012117 | Delivery Sheath |
00811806012100 | Delivery Sheath |
00811806012094 | Delivery Sheath |
00811806011592 | Delivery System |
00811806011585 | Delivery System |
00811806011578 | Delivery System |
00811806011561 | Delivery System |
00811806011509 | Vascular Plug |
00811806011493 | Vascular Plug |
00811806011486 | Vascular Plug |
00811806011479 | Vascular Plug |
00811806011462 | Vascular Plug |
00811806011455 | Vascular Plug |
00811806011448 | Vascular Plug |
00811806010885 | Delivery System |
00811806010878 | Delivery System |
00811806010861 | Delivery System |
00811806010854 | Delivery System |
00811806010847 | Delivery System |
00811806010830 | Delivery System |
00811806010823 | Delivery System |
00811806010816 | Delivery System |
00811806010809 | Delivery System |
00811806010793 | Delivery System |
00811806010786 | Delivery System |
00811806010779 | Delivery System |
00811806010762 | Delivery System |
00811806010755 | Delivery System |
00811806010663 | Exchange System |
00811806010441 | Vascular Plug II |
00811806010434 | Vascular Plug II |
00811806010427 | Vascular Plug II |
00811806010410 | Vascular Plug II |
00811806010403 | Vascular Plug II |
00811806010397 | Vascular Plug II |
00811806010380 | Vascular Plug II |
00811806010373 | Vascular Plug II |
00811806010366 | Vascular Plug II |
00811806010359 | Vascular Plug II |
00811806010342 | Vascular Plug II |
05415067019370 | 9-ASD-038 |
05415067019363 | Septal Occluder |
05415067019356 | Septal Occluder |
05415067019349 | Septal Occluder |
05415067019332 | 9-ASD-030 |
05415067019325 | Septal Occluder |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AMPLATZER 75263094 2144604 Live/Registered |
ST. JUDE MEDICAL, CARDIOLOGY DIVISION, INC. 1997-03-24 |