Catalog Number

56.02.23

Brand Name

Synergetics

Version/Model Number

56.02.23

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

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

MPA

Product Code Name

Endoilluminator

Public Device Record Key

5aee66e9-968d-44a7-8ce1-e3b4ba0736d7

Public Version Date

June 23, 2020

Public Version Number

1

DI Record Publish Date

June 15, 2020

Package DI Number

20841305107124

Quantity per Package

12

Contains DI Package

10841305100647

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box