Catalog Number

3693DGQ

Brand Name

ADC®

Version/Model Number

3693DGQ

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GWZ

Product Code Name

Percussor

Public Device Record Key

1dc8262f-ebc0-4b97-b27f-443dfc465a9b

Public Version Date

June 19, 2020

Public Version Number

3

DI Record Publish Date

September 21, 2016

Package DI Number

00634782546359

Quantity per Package

18

Contains DI Package

00634782046545

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case