FDA UDI In Commercial Distribution 🇺🇸 United States

Serranator

DI: 00852495008104 · Model: FGS-0346-25080 · CAGENT VASCULAR, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Serranator
Primary DI
00852495008104
Version / Model
FGS-0346-25080
Company Name
CAGENT VASCULAR, LLC
Labeler DUNS
009984330
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-13
Public Version
1
Public Version Date
2024-11-21
Public Version Status
New
Public Device Record Key
196826b5-3c2a-4719-b976-e14583a36e52

Device Description

The Serranator® PTA Serration Balloon Catheter is an Over The-Wire (OTW) balloon dilatation catheter designed to perform Percutaneous Transluminal Angioplasty (PTA) for peripheral indications. The Serranator® has a nylon semi- compliant balloon with embedded external metal strips or scoring elements. The unique scoring elements are serrated, designed to create linear, interrupted scoring along the endoluminal surface. This occurs during balloon inflation and is designed to aid arterial expansion.

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
Yes
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
17184 Peripheral angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 00852495008104

Customer Contacts

Phone
9258186875

Device Sizes

Type Value Unit Text
Balloon Diameter 2.5 Millimeter
Balloon Length 80 Millimeter