Catalog Number

-

Brand Name

LiquiBand Flex

Version/Model Number

LBF001

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

December 28, 2018

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

K102076,K102076,K102076

Product Code

MPN

Product Code Name

Tissue Adhesive For The Topical Approximation Of Skin

Public Device Record Key

5870abb4-b33d-4b17-b267-5b9c509c4eb1

Public Version Date

December 28, 2018

Public Version Number

5

DI Record Publish Date

September 06, 2016

Package DI Number

05036912000925

Quantity per Package

6

Contains DI Package

05036912000529

Package Discontinue Date

December 28, 2018

Package Status

Not in Commercial Distribution

Package Type

Shipper Carton