AccessGUDID - DEVICE: AngioSculpt® (00813132021528)

GUDID

Device Identifier (DI) Information

Brand Name: AngioSculpt®
Version or Model: 2237-40100
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 2237-40100
Company Name: Spectranetics Corporation

Primary DI Number: 00813132021528
Issuing Agency: GS1
Commercial Distribution End Date: February 20, 2020
Device Count: 1
Labeler D-U-N-S® Number*: 151047370 *Terms of Use

Device Description: AngioSculpt® PTA Scoring Balloon Catheter

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?
17184	Peripheral angioplasty balloon catheter, basic	A sterile, non-drug-eluting, flexible tube designed for percutaneous transluminal angioplasty (PTA) to dilate a stenotic peripheral (i.e., non-cerebral, non-coronary) artery by controlled inflation of a distensible balloon(s) at its distal tip; it may also be intended for positioning and expansion of a stent/stent-graft. It is available as an over-the-wire (OTW) type with multiple lumens, or a rapid exchange (RX) type with a single lumen. Some types may include cutting/scoring elements (e.g., microsurgical blades, dual wire configurations) to score/modify the plaque. 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: Yes

Sterilization Method [?]
Ethylene Oxide

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: less than 140 Degrees Fahrenheit

Clinically Relevant Size

[?]

Size Type Text
Length: 100 Millimeter
Outer Diameter: 4.0 Millimeter

Device Record Status

Public Device Record Key: a2d0a327-895c-454e-92d4-2d8e195b28dc
Public Version Date: October 26, 2021
Public Version Number: 5
DI Record Publish Date: September 23, 2016