Catalog Number

-

Brand Name

Gongdong

Version/Model Number

GDC-03-F

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

MMK

Product Code Name

Container, Sharps

Public Device Record Key

c4bc3cac-c886-40fb-9a4f-264c72faa214

Public Version Date

August 15, 2022

Public Version Number

1

DI Record Publish Date

August 05, 2022

Package DI Number

16947462492695

Quantity per Package

48

Contains DI Package

06947462492698

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton