Catalog Number

-

Brand Name

OWL®

Version/Model Number

RF22-100-5CS

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

-

Product Code Name

-

Public Device Record Key

aaae3a55-4543-4253-a5f7-6adf857b4ce3

Public Version Date

June 17, 2022

Public Version Number

4

DI Record Publish Date

September 16, 2016

Package DI Number

30381780264518

Quantity per Package

10

Contains DI Package

10381780264514

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX