Catalog Number

GC070CRF

Brand Name

RELIEVA FLEX

Version/Model Number

GC070CRF

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

KAM

Product Code Name

CANNULA, SINUS

Public Device Record Key

1b1894c2-736a-45bb-ba1b-5aea044fc896

Public Version Date

January 22, 2020

Public Version Number

4

DI Record Publish Date

October 01, 2016

Package DI Number

20705031063423

Quantity per Package

5

Contains DI Package

10705031063426

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX