Catalog Number

MP-00019-S

Brand Name

ARROW

Version/Model Number

IPN046487

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

K103658,K103658

Product Code

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

f18a0c74-f147-4dd2-823f-94344104e71d

Public Version Date

February 07, 2019

Public Version Number

5

DI Record Publish Date

September 16, 2016

Package DI Number

30801902077104

Quantity per Package

20

Contains DI Package

00801902077103

Package Discontinue Date

July 12, 2017

Package Status

Not in Commercial Distribution

Package Type

Case