VECTRA®, VASCULAR ACCESS GRAFT - Thoratec Corporation

Duns Number:070156955

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

10002-6040-001

Brand Name

VECTRA®, VASCULAR ACCESS GRAFT

Version/Model Number

10002-6040-001

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

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)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

DSY

Product Code Name

Prosthesis, Vascular Graft, Of 6mm And Greater Diameter

Device Record Status

Public Device Record Key

d74c3f37-286c-4574-ba94-5da3aa647f58

Public Version Date

February 05, 2021

Public Version Number

7

DI Record Publish Date

September 20, 2014

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"THORATEC CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1
2 A medical device with a moderate to high risk that requires special controls. 18
3 A medical device with high risk that requires premarket approval 156