Catalog Number

C-SLRA-SC60

Brand Name

Biodesign

Version/Model Number

G23201

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

K070405,K170945

Product Code

OXE

Product Code Name

Mesh, surgical, collagen, staple line reinforcement

Public Device Record Key

ef0038ea-889f-49f6-851a-3de70c87da14

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 03, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-