Catalog Number

26040

Brand Name

EXEL Syringes

Version/Model Number

26040

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"

Yes

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

-

Product Code

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

fbd02218-cb0a-4993-aca9-97a104e4293e

Public Version Date

September 12, 2018

Public Version Number

3

DI Record Publish Date

September 20, 2016

Package DI Number

20020221260407

Quantity per Package

10

Contains DI Package

10020221260400

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-