Catalog Number

ASA-24103-S

Brand Name

ARROW

Version/Model Number

IPN915661

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

K911260,K911260

Product Code

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

be240fde-d3a1-45b1-8b1a-1eca77bb8f25

Public Version Date

April 21, 2021

Public Version Number

2

DI Record Publish Date

April 28, 2020

Package DI Number

20801902162742

Quantity per Package

5

Contains DI Package

10801902162745

Package Discontinue Date

April 15, 2021

Package Status

Not in Commercial Distribution

Package Type

Case