Catalog Number

CPA00040A

Brand Name

SafeStep

Version/Model Number

CPA00040A

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

Yes

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

-

FDA Premarket Submission

-

Product Code

PTI

Product Code Name

Non-coring (Huber) needle

Public Device Record Key

202c196e-670d-4276-826a-f015b35a4236

Public Version Date

January 13, 2021

Public Version Number

1

DI Record Publish Date

January 05, 2021

Package DI Number

10801741219020

Quantity per Package

5

Contains DI Package

00801741219023

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA