Catalog Number

ASK-05503-BID

Brand Name

ARROW

Version/Model Number

IPN039613

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

Yes

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

-

FDA Premarket Submission

K140110,K140110,K140110

Product Code

BSO

Product Code Name

CATHETER, CONDUCTION, ANESTHETIC

Public Device Record Key

6b878c87-d3bc-434e-ab5d-1d06f4170aa9

Public Version Date

June 29, 2022

Public Version Number

6

DI Record Publish Date

July 17, 2019

Package DI Number

40801902145213

Quantity per Package

5

Contains DI Package

30801902145216

Package Discontinue Date

June 27, 2022

Package Status

Not in Commercial Distribution

Package Type

Case