AccessGUDID - DEVICE: IMPRA® ePTFE Vascular Grafts (00801741021237)

GUDID

Device Identifier (DI) Information

Brand Name: IMPRA® ePTFE Vascular Grafts
Version or Model: 70S04TWC
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 70S04TWC
Company Name: Bard Peripheral Vascular, Inc.

Primary DI Number: 00801741021237
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 135057938 *Terms of Use

Device Description: IMPRA® ePTFE Vascular Graft, Carboflo® Straight Thinwall Carbon-Lined, 4 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, non-medicated	An implantable artificial substitute for a blood vessel intended to replace, bypass or shunt a portion of peripheral vasculature (excludes coronary and cerebral arteries) due to a disease, injury, or for haemodialysis access. It is made of synthetic polymer materials [e.g., woven or knitted polyethylene terephthalate (Dacron) or polytetrafluoroethylene (PTFE) fabrics]; it does not contain any pharmaceuticals and does not incorporate a metallic mesh (i.e., it is not a stent-graft).	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: Inner Diameter, 4 Millimeter
Length: 70 Centimeter

Device Record Status

Public Device Record Key: 5c452b83-de2c-4013-8494-fa62787ec382
Public Version Date: December 25, 2025
Public Version Number: 5
DI Record Publish Date: May 08, 2015