Catalog Number

S30ML

Brand Name

RELI®

Version/Model Number

S30ML

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

52ca3341-fb94-4873-b03a-42131ea77cd3

Public Version Date

May 09, 2022

Public Version Number

1

DI Record Publish Date

May 01, 2022

Package DI Number

10386120012152

Quantity per Package

40

Contains DI Package

00386120012155

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Carton