Catalog Number

8198

Brand Name

CONVERTORS

Version/Model Number

8198

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

PUI

Product Code Name

Drape, surgical, exempt

Public Device Record Key

03085321-f020-4234-a8dc-361c0ef2ca53

Public Version Date

December 22, 2021

Public Version Number

3

DI Record Publish Date

December 11, 2018

Package DI Number

50885380165717

Quantity per Package

10

Contains DI Package

10885380165719

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE