AccessGUDID - DEVICE: taperflo™ (05037881009681)

GUDID

Device Identifier (DI) Information

Brand Name: taperflo™
Version or Model: W20ST0407S
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: W20ST0407S
Company Name: VASCUTEK LTD

Primary DI Number: 05037881009681
Issuing Agency: GS1
Commercial Distribution End Date: March 30, 2019
Device Count: 1
Labeler D-U-N-S® Number*: 229053087 *Terms of Use

Device Description: taperflo Gelatin Sealed ePTFE Vascular Prosthesis Stepped Taper with Wrap

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 a diseased or injured vessel, typically the aorta, an iliac, a femoral or popliteal artery; it is not intended for use in the coronary arteries. It is typically made of woven or knitted polyethylene terephthalate (Dacron) or polytetrafluoroethylene (PTFE) fabrics; it does not incorporate a metallic mesh (i.e., it is not a stent-graft).	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
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
Special Storage Condition, Specify: Store in clean, dry area at room temperature. Do not expose ePTFE products to temperature greater than 500°F (260 °C).

Clinically Relevant Size

[?]

Size Type Text
Length: 20 Centimeter
Device Size Text, specify: Diameter 4-7 mm

Device Record Status

Public Device Record Key: fbb12633-1ed4-4d02-94d7-ab4a208b9472
Public Version Date: September 24, 2025
Public Version Number: 8
DI Record Publish Date: October 19, 2015