Catalog Number

ASA-24101-GS

Brand Name

ARROW

Version/Model Number

IPN040075

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

K931644,K931644

Product Code

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

be15e7ab-9da6-4412-89f9-fdb3e3f335a2

Public Version Date

April 21, 2021

Public Version Number

4

DI Record Publish Date

October 15, 2018

Package DI Number

60801902113988

Quantity per Package

5

Contains DI Package

50801902113981

Package Discontinue Date

April 15, 2021

Package Status

Not in Commercial Distribution

Package Type

Case