Catalog Number

-

Brand Name

Gentle Vac

Version/Model Number

17420

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 31, 2019

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

HDB

Product Code Name

Extractor, Vacuum, Fetal

Public Device Record Key

322c6227-ae3a-4508-8a1e-9ef216cd1d5d

Public Version Date

February 21, 2019

Public Version Number

4

DI Record Publish Date

March 20, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-