Catalog Number

-

Brand Name

Circumplast

Version/Model Number

Circumplast 11mm Shipping Carton

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

K151095,K151095

Product Code

HFX

Product Code Name

Clamp, Circumcision

Public Device Record Key

ea54716d-2409-40c4-8184-4641ffaa7a88

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

October 18, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-