Catalog Number

OP2528-001

Brand Name

V. Mueller

Version/Model Number

OP2528-001

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 15, 2021

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

HNI

Product Code Name

Retractor, ophthalmic

Public Device Record Key

85972c5f-ac23-4156-adfe-18e69a2930e0

Public Version Date

March 07, 2022

Public Version Number

2

DI Record Publish Date

December 27, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-