AccessGUDID - DEVICE: UltraClip® Dual Trigger Breast Tissue Marker (00801741032233)

GUDID

Device Identifier (DI) Information

Brand Name: UltraClip® Dual Trigger Breast Tissue Marker
Version or Model: 863017D
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 863017D
Company Name: Bard Peripheral Vascular, Inc.

Primary DI Number: 00801741032233
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 135057938 *Terms of Use

Device Description: ULTRACLIP® DUAL TRIGGER breast tissue marker 17g x 10cm needle, Ultrasound Enhanced Titanium Ribbon

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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?
40808	Radiological image marker, implantable	A device intended to be implanted within the body, either temporarily or permanently, to create identifying marks that can be seen on radiographic film or digital images. It is typically in the form of a wire, needle, bead, clip, stent-like tube, washer or fluid, and used to locate and delineate a tumour, lesion, or other site of interest. It is made from materials compatible with the imaging system with which it is intended to be used [e.g., magnetic resonance imaging (MRI), x-ray, or nuclear medicine]; it may be intended for use during radiotherapy procedures.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
NEU	MARKER, RADIOGRAPHIC, IMPLANTABLE

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
Device Size Text, specify: Needle Length, 10 Centimeter
Needle Gauge: 17 Gauge

Device Record Status

Public Device Record Key: 22990143-972a-4492-8b88-27fe35d638d0
Public Version Date: September 18, 2023
Public Version Number: 4
DI Record Publish Date: September 25, 2015