Catalog Number

LBLSTNDGSM

Brand Name

MEDLINE

Version/Model Number

LBLSTNDGSM

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

LYV

Product Code Name

LABEL OR TAG, STERILE

Public Device Record Key

c15c6cb8-2fb1-45e7-a099-d11283771ad7

Public Version Date

January 10, 2022

Public Version Number

1

DI Record Publish Date

January 01, 2022

Package DI Number

40884389239385

Quantity per Package

80

Contains DI Package

10884389239384

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE