Catalog Number

406056

Brand Name

N/A

Version/Model Number

406056

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"

-

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

6a99049f-997b-4c5f-a62c-92f88b1e8a0f

Public Version Date

July 22, 2019

Public Version Number

3

DI Record Publish Date

September 16, 2016

Package DI Number

50382904060560

Quantity per Package

10

Contains DI Package

00382904060565

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case