Catalog Number

31145660

Brand Name

Devon

Version/Model Number

31145660

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

DXC

Product Code Name

CLAMP, VASCULAR

Public Device Record Key

eaf9023d-3196-4dff-9d43-cf2c722fc738

Public Version Date

September 10, 2019

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

10884521152069

Quantity per Package

200

Contains DI Package

20884521152066

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE