Catalog Number

-

Brand Name

ButtonHole SINGLE NEEDLE SET

Version/Model Number

BH-3006

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

FIE

Product Code Name

Needle, Fistula

Public Device Record Key

a72d3da2-52e6-454d-b80a-15b3fa6e4068

Public Version Date

July 14, 2020

Public Version Number

1

DI Record Publish Date

July 06, 2020

Package DI Number

10842289102993

Quantity per Package

30

Contains DI Package

00842289102996

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Box