Minnie® support catheter
GUDID M20657020
The Minnie support catheters are intended to be used in conjunction with steerable guidewires in order to access discrete regions of the arterial and/or coronary vasculature. They may be used to facilitate placement and exchange of guidewires and other interventional devices. The Minnie support catheters also may be used to subselectively infuse/deliver therapeutic agents.
Vascular Solutions, Inc.
Peripheral vascular infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter| Primary Device ID | M20657020 |
| NIH Device Record Key | c01adf22-b0c8-4f90-a269-aad15d613d9b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Minnie® support catheter |
| Version Model Number | 5702 |
| Company DUNS | 008999906 |
| Company Name | Vascular Solutions, Inc. |
| 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 | 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 |
Customer Support Contacts
Device Dimensions
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
| Device Size Text, specify | 0 |
| Length | 90 Centimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | M20657020 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K082337
FDA Product Code
| DQY | Catheter, Percutaneous |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-11-11 |
| Device Publish Date | 2016-09-05 |
On-Brand Devices [Minnie® support catheter]
| M20657130 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657120 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657110 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657100 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657080 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657070 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657060 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657050 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657040 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657030 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657020 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657010 | The Minnie support catheters are intended to be used in conjunction with steerable guidewires in |
| M20657000 | 5700 |
Trademark Results [Minnie]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MINNIE 97298744 not registered Live/Pending |
New Ravenna, LLC 2022-03-07 |
 MINNIE 87510751 not registered Live/Pending |
Perkin & Perkin, LLC 2017-06-29 |
 MINNIE 86840641 not registered Dead/Abandoned |
Edie Parker LLC 2015-12-06 |
 MINNIE 85593419 4401042 Live/Registered |
Winnebago Industries, Inc. 2012-04-10 |
 MINNIE 77818971 3752325 Live/Registered |
TELEFLEX INNOVATIONS S.Ã R.L. 2009-09-02 |
 MINNIE 76428013 3477059 Dead/Cancelled |
Segal, Jonathan 2002-07-08 |
 MINNIE 74684692 1982412 Dead/Cancelled |
WINNEBAGO INDUSTRIES, INC. 1995-06-05 |
 MINNIE 72229371 0812855 Dead/Expired |
PARAGON SPRING COMPANY 1965-10-05 |
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