Catalog Number

-

Brand Name

McKesson

Version/Model Number

16-PBSL17G

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FMK

Product Code Name

Lancet, Blood

Public Device Record Key

f5b295b9-d09c-4f47-9434-810c137785d7

Public Version Date

July 08, 2021

Public Version Number

2

DI Record Publish Date

July 14, 2020

Package DI Number

00612479185333

Quantity per Package

20

Contains DI Package

00612479185326

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case