Catalog Number

-

Brand Name

WEGO

Version/Model Number

3ml

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

K072739,K072739,K072739

Product Code

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

49b6e5c8-3688-4b71-b070-c3f070edf53d

Public Version Date

January 08, 2021

Public Version Number

1

DI Record Publish Date

December 31, 2020

Package DI Number

26932992110598

Quantity per Package

100

Contains DI Package

16932992110591

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX