Catalog Number

ASK-04001-GFH-S

Brand Name

ARROW

Version/Model Number

IPN032688

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

Yes

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

-

FDA Premarket Submission

-

Product Code

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

364fe831-4479-454c-ba6a-5ea4f66e7653

Public Version Date

November 13, 2019

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

30801902098277

Quantity per Package

5

Contains DI Package

00801902098276

Package Discontinue Date

November 12, 2019

Package Status

Not in Commercial Distribution

Package Type

Case