Catalog Number

-

Brand Name

LiquiBand XL

Version/Model Number

72014019

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

K211878,K211878,K211878

Product Code

OMD

Product Code Name

Cutaneous Tissue Adhesive With Mesh

Public Device Record Key

f16f4d1a-14a3-4095-9749-f89415c545df

Public Version Date

June 08, 2022

Public Version Number

1

DI Record Publish Date

May 31, 2022

Package DI Number

05036912001243

Quantity per Package

2

Contains DI Package

05036912001250

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton