Catalog Number

MH-05503-1

Brand Name

ARROW

Version/Model Number

IPN046438

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

-

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

-

FDA Premarket Submission

K140110,K140110

Product Code

BSO

Product Code Name

CATHETER, CONDUCTION, ANESTHETIC

Public Device Record Key

0ccde803-b597-4575-b436-577d1dd32498

Public Version Date

May 24, 2022

Public Version Number

7

DI Record Publish Date

October 09, 2018

Package DI Number

50801902042458

Quantity per Package

10

Contains DI Package

40801902042451

Package Discontinue Date

May 20, 2022

Package Status

Not in Commercial Distribution

Package Type

Box