Catalog Number

-

Brand Name

RapidVac

Version/Model Number

SEA3700

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

-

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

-

Product Code

FYD

Product Code Name

APPARATUS, EXHAUST, SURGICAL

Public Device Record Key

2022fd2f-058b-4296-8477-98261a94aa26

Public Version Date

April 20, 2021

Public Version Number

3

DI Record Publish Date

September 24, 2016

Package DI Number

20884524001422

Quantity per Package

2

Contains DI Package

10884524001425

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE