Catalog Number

NDL-100-32

Brand Name

Needle

Version/Model Number

NDL-100-32

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

-

Product Code

DWS

Product Code Name

Instruments, Surgical, Cardiovascular

Public Device Record Key

d5bdbb83-c9d0-463b-b5c6-0ea5ec036366

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

August 09, 2017

Package DI Number

20841268102709

Quantity per Package

100

Contains DI Package

10841268102702

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Sipper Box