AccessGUDID - DEVICE: Diamondback Coronary (10852528005701)

GUDID

Device Identifier (DI) Information

Brand Name: Diamondback Coronary
Version or Model: GWC-12325LG-FT
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 7-10038-01
Company Name: Cardiovascular Systems, Inc.

Primary DI Number: 10852528005701
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 024954518 *Terms of Use

Device Description: Guidewire, Viperwire Advance Coronary Flex Tip .014: dia, .012" 1 Pack 325 cm

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?
35094	Cardiac/peripheral vascular guidewire, single-use	A long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
MCX	Catheter, Coronary, Atherectomy

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: Length 325 cm
Device Size Text, specify: Max Shaft Diameter 0.012 inches
Device Size Text, specify: Max Tip Diameter: 0.014 inches

Device Record Status

Public Device Record Key: 79398385-74c2-4219-88c8-5994baa83f71
Public Version Date: December 18, 2023
Public Version Number: 2
DI Record Publish Date: September 23, 2019