Catalog Number

-

Brand Name

Alleset

Version/Model Number

Model 25-3011

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

FTA

Product Code Name

Light, surgical, accessories

Public Device Record Key

44b5dc0e-3925-4c29-9dbf-87aa15eb19e2

Public Version Date

March 16, 2021

Public Version Number

1

DI Record Publish Date

March 08, 2021

Package DI Number

26931918127306

Quantity per Package

1

Contains DI Package

16931918127309

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton