Catalog Number

-

Brand Name

ULTRA FLOW

Version/Model Number

8065751795

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

-

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

NKK

Product Code Name

NEEDLE, HYPODERMIC, SINGLE LUMEN, REPROCESSED

Public Device Record Key

7b3321ed-ec03-4b3b-b59a-ab0c2ef5574d

Public Version Date

October 07, 2019

Public Version Number

6

DI Record Publish Date

June 07, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-