Catalog Number

ASA-24090-GS

Brand Name

ARROW

Version/Model Number

IPN040069

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

K931644,K931644

Product Code

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

41e2b6a0-7212-4b45-86be-7f0f010c7f05

Public Version Date

July 22, 2019

Public Version Number

5

DI Record Publish Date

September 16, 2016

Package DI Number

40801902126175

Quantity per Package

5

Contains DI Package

10801902126174

Package Discontinue Date

October 02, 2018

Package Status

Not in Commercial Distribution

Package Type

Case