Catalog Number

SNAPEVAC01

Brand Name

SNAPEVAC

Version/Model Number

SNAPEVAC01

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 07, 2022

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

-

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

50ac93dc-be86-4a3c-b02c-e9fe5fea4e0e

Public Version Date

June 08, 2022

Public Version Number

2

DI Record Publish Date

June 06, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-