Catalog Number

-

Brand Name

ID Adapter

Version/Model Number

5070204

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)

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

ec4be519-0042-4722-b364-b88b24aa49a5

Public Version Date

June 17, 2022

Public Version Number

8

DI Record Publish Date

November 18, 2016

Package DI Number

27290108240904

Quantity per Package

320

Contains DI Package

07290108240900

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-