Catalog Number

SE5623

Brand Name

Synergetics

Version/Model Number

SE5623

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

HQE

Product Code Name

Instrument, vitreous aspiration and cutting, ac-powered

Public Device Record Key

7faf47e4-9f6a-4843-b386-7b8f82e9948a

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 01, 2017

Package DI Number

20841305111428

Quantity per Package

6

Contains DI Package

10841305111414

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box