AccessGUDID - DEVICE: FLEX Vessel Prep System (00863656000301)

GUDID

Device Identifier (DI) Information

Brand Name: FLEX Vessel Prep System
Version or Model: FSC 4-120
Commercial Distribution Status: In Commercial Distribution
Catalog Number: FSC 4-120
Company Name: Venturemed Group, Inc.

Primary DI Number: 00863656000301
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 027796091 *Terms of Use

Device Description: FLEX Vessel Prep System, FSC 4-120

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
44088	Coronary angioplasty balloon catheter, cutting/scoring	A sterile, flexible tube designed for use in percutaneous transluminal coronary angioplasty (PTCA) to dilate a stenotic coronary artery and increase myocardial perfusion, by controlled inflation of a distensible balloon at its distal tip with peripheral cutting/scoring elements (e.g., microsurgical atherotomes) intended to remove stenotic material. The device is typically placed using a guidewire and guiding catheter, and its balloon is inflated by the infusion of liquid through it tubular body. The tube and balloon are typically made of polymer materials and the cutting/scoring elements are typically made of metal [e.g., nickel-titanium alloy (Nitinol)]. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
PNO	Catheter, Percutaneous, Cutting/Scoring

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: a8e9f55d-a9fa-4ff4-bd95-410d9cd18a38
Public Version Date: April 21, 2023
Public Version Number: 3
DI Record Publish Date: June 27, 2019