Catalog Number

1281.A

Brand Name

Backflush Instrument with 20G / 0.9 mm blunt needle

Version/Model Number

1281.A

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

-

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

GDM

Product Code Name

Needle, Aspiration And Injection, Reusable

Public Device Record Key

5966caea-7a77-4b1e-bbb1-1e5744a8d061

Public Version Date

February 22, 2021

Public Version Number

2

DI Record Publish Date

November 16, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-