Catalog Number

26061

Brand Name

Exel Allergy Syringes

Version/Model Number

26061

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

K861153,K861153,K861153

Product Code

FMF

Product Code Name

Syringe, Piston

Public Device Record Key

19848fed-fdb4-4d20-9f8c-da623392ca44

Public Version Date

September 12, 2018

Public Version Number

4

DI Record Publish Date

September 23, 2016

Package DI Number

20020221260612

Quantity per Package

40

Contains DI Package

10020221260615

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-