Catalog Number

-

Brand Name

NAMIC

Version/Model Number

80751003

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

DTL

Product Code Name

ADAPTOR, STOPCOCK, MANIFOLD, FITTING, CARDIOPULMONARY BYPASS

Public Device Record Key

ededd450-33ee-4566-8efe-965a3f49d221

Public Version Date

April 05, 2019

Public Version Number

3

DI Record Publish Date

September 17, 2015

Package DI Number

H965807510031

Quantity per Package

10000

Contains DI Package

H965807510030

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX