Catalog Number

-

Brand Name

Spine Needle (18 Gauge)

Version/Model Number

DFX-N8/1

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

BSP

Product Code Name

Needle, Conduction, Anesthetic (W/Wo Introducer)

Public Device Record Key

974809ce-f3bf-4274-b07c-f6045d1f0974

Public Version Date

November 06, 2020

Public Version Number

7

DI Record Publish Date

September 22, 2016

Package DI Number

00846338001469

Quantity per Package

10

Contains DI Package

00846338000776

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box (DFX-N8)