Catalog Number

FFA 50

Brand Name

Female - Female Adapter

Version/Model Number

FFA 50

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"

Yes

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

K980417,K980417

Product Code

LNH

Product Code Name

System, Nuclear Magnetic Resonance Imaging

Public Device Record Key

f4e0e04d-1733-4f50-ba23-51886c8846a3

Public Version Date

February 19, 2021

Public Version Number

2

DI Record Publish Date

October 25, 2019

Package DI Number

40616258021667

Quantity per Package

50

Contains DI Package

00616258021669

Package Discontinue Date

December 31, 9999

Package Status

In Commercial Distribution

Package Type

-