Catalog Number

GE12023

Brand Name

Biotronix Healthcare Syringes

Version/Model Number

GE12023

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

762aacba-996d-4455-b6da-10dc28e2bef6

Public Version Date

October 17, 2022

Public Version Number

4

DI Record Publish Date

October 12, 2019

Package DI Number

20858835007312

Quantity per Package

8

Contains DI Package

10858835007315

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case