Catalog Number

-

Brand Name

Wire Electrode Needle Set Female

Version/Model Number

1512A-F

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

FEN

Product Code Name

DEVICE, CYSTOMETRIC, HYDRAULIC

Public Device Record Key

b0e0939e-b184-47ac-bc53-0e98b9a834bb

Public Version Date

June 11, 2018

Public Version Number

3

DI Record Publish Date

September 21, 2016

Package DI Number

20627825000493

Quantity per Package

560

Contains DI Package

10627825000496

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-