AccessGUDID - DEVICE: IMPRA® ePTFE Vascular Grafts (00801741023347)

GUDID

Device Identifier (DI) Information

Brand Name: IMPRA® ePTFE Vascular Grafts
Version or Model: F70T85TWS
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: F70T85TWS
Company Name: Bard Peripheral Vascular, Inc.

Primary DI Number: 00801741023347
Issuing Agency: GS1
Commercial Distribution End Date: September 30, 2024
Device Count: 1
Labeler D-U-N-S® Number*: 135057938 *Terms of Use

Device Description: IMPRA® ePTFE Vascular Graft, Flex™ Thinwall Tapered Small Beading, 8-5 mm x 70 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":	Yes
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?
35281	Synthetic vascular graft	An implantable artificial substitute for a blood vessel intended to replace or bypass the diseased or injured vessel. It is typically made of woven or knitted polyethylene terephthalate (Dacron) or polytetrafluoroethylene (PTFE) fabrics and is best suited for large (more than 10 mm) diameter, high-flow vessel replacement (e.g., aortic or aorto-iliac artery reconstruction) and also for haemodialysis access and extra-anatomic bypass grafting. The device is used in many vascular bypass procedures (e.g., aorto-iliac, femoral-popliteal, axillo-axillary artery) except those involving the coronary arteries.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
DYF	PROSTHESIS, VASCULAR GRAFT, OF LESS THEN 6MM DIAMETER
DSY	PROSTHESIS, VASCULAR GRAFT, OF 6MM AND GREATER DIAMETER

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: Internal Diameter, Tapered, 8-5 Millimeter
Length: 70 Centimeter

Device Record Status

Public Device Record Key: 6347572b-4a81-48bc-a7a8-e86ba0be1416
Public Version Date: December 10, 2024
Public Version Number: 4
DI Record Publish Date: April 29, 2015