Catalog Number

-

Brand Name

Care Touch

Version/Model Number

LLS3ml

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)

-

Over the Counter (OTC)

Yes

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

afdceeac-fe42-4334-8bc3-3183bc21f462

Public Version Date

June 17, 2019

Public Version Number

4

DI Record Publish Date

August 31, 2016

Package DI Number

10370393518015

Quantity per Package

12

Contains DI Package

00370393518018

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-