Catalog Number

OB-1000

Brand Name

N/A

Version/Model Number

OB-1000

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

HFX

Product Code Name

CLAMP, CIRCUMCISION

Public Device Record Key

943ebe0e-e97b-4140-ba42-2945d69d270f

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 30, 2016

Package DI Number

50885403108349

Quantity per Package

10

Contains DI Package

10885403108341

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case