Catalog Number

3948

Brand Name

BOEHRINGER® VAVD VacPac

Version/Model Number

3948

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

KDP

Product Code Name

Regulator, Vacuum

Public Device Record Key

edeb2988-19b0-4d3b-9d2d-3290166b27f7

Public Version Date

June 22, 2022

Public Version Number

3

DI Record Publish Date

July 01, 2018

Package DI Number

70816286020804

Quantity per Package

10

Contains DI Package

10816286020802

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box