Catalog Number

-

Brand Name

CONMED

Version/Model Number

1222

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 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"

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

-

Product Code

GCJ

Product Code Name

Laparoscope, General & Plastic Surgery

Public Device Record Key

da9bc044-88f1-4e6d-87ab-d1e545a522a7

Public Version Date

January 09, 2020

Public Version Number

3

DI Record Publish Date

March 22, 2019

Package DI Number

20412786063188

Quantity per Package

10

Contains DI Package

10412786063181

Package Discontinue Date

October 31, 2019

Package Status

Not in Commercial Distribution

Package Type

Carton