Catalog Number

EPK2305-01

Brand Name

EndoClot PHS

Version/Model Number

EPK2305

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

-

Product Code Name

-

Public Device Record Key

fc663d56-fcdd-4e1e-8bfd-0e9efcd05f43

Public Version Date

November 16, 2021

Public Version Number

2

DI Record Publish Date

June 23, 2021

Package DI Number

26972011720032

Quantity per Package

1

Contains DI Package

16972011720035

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-