Catalog Number

FD+162530BCR-CAP

Brand Name

NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER

Version/Model Number

16GX1" HTC-30W-D-CAP

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"

-

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

FIE

Product Code Name

Needle, fistula

Public Device Record Key

803d00f8-572d-48ec-98ae-cf3d0a637d9f

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

April 01, 2016

Package DI Number

40383790001326

Quantity per Package

10

Contains DI Package

10383790001325

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case