Catalog Number

26703

Brand Name

EXEL Scalp Vein Set

Version/Model Number

26703

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"

Yes

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

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

332f8a13-6e7f-466d-9273-c06abcf7eee5

Public Version Date

July 23, 2020

Public Version Number

4

DI Record Publish Date

September 20, 2016

Package DI Number

20020221267031

Quantity per Package

10

Contains DI Package

10020221267034

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-