FDA UDI Not in Commercial Distribution 🇺🇸 United States

Pronto® V3 extraction catheter

DI: M20650030 · Model: 5003 · Vascular Solutions, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Pronto® V3 extraction catheter
Primary DI
M20650030
Version / Model
5003
Company Name
Vascular Solutions, Inc.
Labeler DUNS
008999906
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-05
Public Version
7
Public Version Date
2023-06-06
Public Version Status
Update
Public Device Record Key
be8e364d-4ac9-48cc-abe1-bb4e78b4dbc5
Distribution End Date
2022-04-01

Device Description

The Pronto catheter is indicated for the removal of fresh, soft emboli and thrombi from vessels in the coronary and peripheral vasculature.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QEZ Aspiration Thrombectomy Catheter

GMDN Terms

Code Name
58173 Thrombectomy suction catheter

Identifiers

Type ID
Primary M20650030

Customer Contacts

Phone
888-240-6001

Device Sizes

Type Value Unit Text
Catheter Gauge 6 French