Catalog Number

-

Brand Name

N/A

Version/Model Number

DGP-PM2

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"

Yes

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

K203494,K203494,K203494

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

ed8e5ded-c4d1-497d-a3d6-4965cc72f8ac

Public Version Date

June 29, 2022

Public Version Number

2

DI Record Publish Date

March 17, 2021

Package DI Number

35060441917615

Quantity per Package

5

Contains DI Package

15060441917611

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box