Catalog Number

2201

Brand Name

Swann Morton Ltd.

Version/Model Number

SKIN GRAFT BLADES SG3

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

FZW

Product Code Name

Expander, Surgical, Skin Graft

Public Device Record Key

ffe4fc81-3652-48b7-8ae7-300095913d7c

Public Version Date

May 10, 2022

Public Version Number

1

DI Record Publish Date

May 02, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-