Catalog Number

10-0580

Brand Name

MIKULICZ CLAMP

Version/Model Number

10-0580

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

-

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

FFR

Product Code Name

DEVICE, LOCKING, FOR INTESTINAL CLAMP

Public Device Record Key

1c402489-d85e-43ea-8075-b7c4ea8c7a01

Public Version Date

October 15, 2018

Public Version Number

1

DI Record Publish Date

September 12, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-