Catalog Number

-

Brand Name

Care Touch

Version/Model Number

HH-X-T, IC

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

QRK

Product Code Name

Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

Public Device Record Key

47f2c74b-9a4f-4912-8d81-8342831e46db

Public Version Date

August 22, 2022

Public Version Number

1

DI Record Publish Date

August 12, 2022

Package DI Number

20810011730377

Quantity per Package

2020

Contains DI Package

10810011730370

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

inner case