ASSURANT® COBALT
GUDID 00613994931054
Stent ASC760SV AssrntCo 7mmx60mmx80cm
MEDTRONIC, INC.
Iliac artery stent, bare-metal| Primary Device ID | 00613994931054 |
| NIH Device Record Key | 12e85829-014e-4066-8642-7ed8570ace10 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ASSURANT® COBALT |
| Version Model Number | ASC760SV |
| Company DUNS | 006261481 |
| Company Name | MEDTRONIC, INC. |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Length | 60 Millimeter |
| Length | 60 Millimeter |
| Length | 60 Millimeter |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
| Device Size Text, specify | 0 |
| Length | 60 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00613994931054 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Approval: P110011
FDA Product Code
| NIO | STENT, ILIAC |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2014-09-23 |
On-Brand Devices [ASSURANT® COBALT]
| 00613994931283 | Stent ASC730LV AssrntCo 7mmx30mmx130cm |
| 00613994931276 | Stent ASC720SV AssrntCo 7mmx20mmx80cm |
| 00613994931269 | Stent ASC720LV AssrntCo 7mmx20mmx130cm |
| 00613994931252 | Stent ASC660SV AssrntCo 6mmx60mmx80cm |
| 00613994931245 | Stent ASC640SV AssrntCo 6mmx40mmx80cm |
| 00613994931238 | Stent ASC630SV AssrntCo 6mmx30mmx80cm |
| 00613994931221 | Stent ASC630LV AssrntCo 6mmx30mmx130cm |
| 00613994931214 | Stent ASC620SV AssrntCo 6mmx20mmx80cm |
| 00613994931207 | Stent ASC620LV AssrntCo 6mmx20mmx130cm |
| 00613994931191 | Stent ASC1060SV AssrntCo 10mmx60mmx80cm |
| 00613994931184 | Stent ASC1040SV AssrntCo 10mmx40mmx80cm |
| 00613994931177 | Stent ASC1030SV AssrntCo 10mmx30mmx80cm |
| 00613994931160 | Stent ASC1030LV AssrntCo 10mmx30mmx130cm |
| 00613994931153 | Stent ASC960SV AssrntCo 9mmx60mmx80cm |
| 00613994931146 | Stent ASC940SV AssrntCo 9mmx40mmx80cm |
| 00613994931139 | Stent ASC930SV AssrntCo 9mmx30mmx80cm |
| 00613994931122 | Stent ASC930LV AssrntCo 9mmx30mmx130cm |
| 00613994931115 | Stent ASC860SV AssrntCo 8mmx60mmx80cm |
| 00613994931108 | Stent ASC840SV AssrntCo 8mmx40mmx80cm |
| 00613994931092 | Stent ASC830SV AssrntCo 8mmx30mmx80cm |
| 00613994931085 | Stent ASC830LV AssrntCo 8mmx30mmx130cm |
| 00613994931078 | Stent ASC820SV AssrntCo 8mmx20mmx80cm |
| 00613994931061 | Stent ASC820LV AssrntCo 8mmx20mmx130cm |
| 00613994931054 | Stent ASC760SV AssrntCo 7mmx60mmx80cm |
| 00613994931047 | Stent ASC740SV AssrntCo 7mmx40mmx80cm |
| 00613994931030 | Stent ASC730SV AssrntCo 7mmx30mmx80cm |
Trademark Results [ASSURANT]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ASSURANT 97976045 not registered Live/Pending |
Knowledge Based Systems, Inc 2022-05-20 |
 ASSURANT 97421269 not registered Live/Pending |
Knowledge Based Systems, Inc 2022-05-20 |
 ASSURANT 85278299 4203111 Live/Registered |
Watlow Electric Manufacturing Company 2011-03-28 |
 ASSURANT 78606599 not registered Dead/Abandoned |
Assurant, Inc. 2005-04-12 |
 ASSURANT 78606598 3349515 Live/Registered |
Assurant, Inc. 2005-04-12 |
 ASSURANT 78606596 3349514 Dead/Cancelled |
Assurant, Inc. 2005-04-12 |
 ASSURANT 78396894 3107738 Live/Registered |
Assurant, Inc. 2004-04-06 |
 ASSURANT 78350081 3114932 Dead/Cancelled |
Assurant, Inc. 2004-01-09 |
 ASSURANT 78349997 3124333 Live/Registered |
Assurant, Inc. 2004-01-09 |
 ASSURANT 78078526 2655089 Live/Registered |
ASSURANT, INC. 2001-08-09 |
 ASSURANT 75769638 2543367 Live/Registered |
ASSURANT, INC. 1999-08-06 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.