FDA UDI In Commercial Distribution 🇺🇸 United States

FLEX Vessel Prep System

DI: 00863656000325 · Model: FSC 4-75 · Venturemed Group, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FLEX Vessel Prep System
Primary DI
00863656000325
Version / Model
FSC 4-75
Catalog Number
FSC 4-75
Company Name
Venturemed Group, Inc.
Labeler DUNS
027796091
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-03
Public Version
2
Public Version Date
2023-04-21
Public Version Status
Update
Public Device Record Key
1c32e000-db71-407a-a57e-1595acc01418

Device Description

FLEX Vessel Prep System, FSC 4-75

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
PNO Catheter, Percutaneous, Cutting/Scoring

GMDN Terms

Code Name
44088 Coronary angioplasty balloon catheter, cutting/scoring

Identifiers

Type ID
Primary 00863656000325

Device Sizes

Type Value Unit Text
Catheter Length 75 Centimeter