Primary Device ID | 10886704071747 |
NIH Device Record Key | 4d96a4f6-15bf-4b7c-89c2-6fba0fc06182 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CERENOVUS ENTERPRISE |
Version Model Number | ENF451400 |
Catalog Number | ENF451400 |
Company DUNS | 482661753 |
Company Name | Medos International Sàrl |
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 |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Special Storage Condition, Specify | Between 0 and 0 *Do not use if opened or damaged. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10886704071747 [Primary] |
NJE | intracranial neurovascular stent |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2021-02-05 |
Device Publish Date | 2014-09-20 |
10886704075400 | CERENOVUS ENTERPRISE 2 Vascular Reconstruction Device Stent OD (mm) 4.0 Stent Length (mm) 39 NO |
10886704075394 | CERENOVUS ENTERPRISE 2 Vascular Reconstruction Device Stent OD (mm) 4.0 Stent Length (mm) 39 Rec |
10886704075387 | CERENOVUS ENTERPRISE 2 Vascular Reconstruction Device Stent OD (mm) 4.0 Stent Length (mm) 30 NO |
10886704075370 | CERENOVUS ENTERPRISE 2 Vascular Reconstruction Device Stent OD (mm) 4.0 Stent Length (mm) 30 Rec |
10886704075363 | CERENOVUS ENTERPRISE 2 Vascular Reconstruction Device Stent OD (mm) 4.0 Stent Length (mm) 23 NO |
10886704075356 | CERENOVUS ENTERPRISE 2 Vascular Reconstruction Device Stent OD (mm) 4.0 Stent Length (mm) 23 Rec |
10886704075349 | CERENOVUS ENTERPRISE 2 Vascular Reconstruction Device Stent OD (mm) 4.0 Stent Length (mm) 16 NO |
10886704075332 | CERENOVUS ENTERPRISE 2 Vascular Reconstruction Device Stent OD (mm) 4.0 Stent Length (mm) 16 Rec |
10886704071808 | CERENOVUS ENTERPRISE Vascular Reconstruction Device and Delivery System Unconstrained Stent OD 4 |
10886704071785 | CERENOVUS ENTERPRISE Vascular Reconstruction Device and Delivery System Unconstrained Stent OD 4 |
10886704071761 | CERENOVUS ENTERPRISE Vascular Reconstruction Device and Delivery System Unconstrained Stent OD 4 |
10886704071747 | CERENOVUS ENTERPRISE Vascular Reconstruction Device and Delivery System Unconstrained Stent OD 4 |
10886704044048 | CERENOVUS ENTERPRISE Vascular Reconstruction Device and Delivery System Unconstrained Stent OD 4 |
10886704044031 | CERENOVUS ENTERPRISE Vascular Reconstruction Device and Delivery System Unconstrained Stent OD 4 |
10886704044024 | CERENOVUS ENTERPRISE Vascular Reconstruction Device and Delivery System Unconstrained Stent OD 4 |
10886704044017 | CERENOVUS ENTERPRISE Vascular Reconstruction Device and Delivery System Unconstrained Stent OD 4 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CERENOVUS ENTERPRISE 87643525 not registered Live/Pending |
Johnson & Johnson 2017-10-12 |