Catalog Number

C-000.32.537

Brand Name

LENS COVERS

Version/Model Number

C-000.32.537

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 21, 2020

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

FSP

Product Code Name

LOUPE, DIAGNOSTIC/SURGICAL

Public Device Record Key

0cc2b742-3f42-4e45-93cb-a2f33bd3c7fc

Public Version Date

December 22, 2020

Public Version Number

2

DI Record Publish Date

September 17, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-