Catalog Number

96-108-17111

Brand Name

Mergence™-S

Version/Model Number

96-108-17111

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

-

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

K103033

Product Code

HTR

Product Code Name

RASP

Public Device Record Key

93791a57-e40a-4ee1-a7b0-1e88c9c5e148

Public Version Date

June 04, 2020

Public Version Number

4

DI Record Publish Date

September 20, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-