Catalog Number

S1160BA-RPL

Brand Name

Schuco

Version/Model Number

S1160BA-RPL

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

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

KDQ

Product Code Name

Bottle, Collection, Vacuum

Public Device Record Key

3dc8d6f4-cb8b-4673-8f95-9cd23ec3f535

Public Version Date

January 08, 2021

Public Version Number

7

DI Record Publish Date

September 12, 2016

Package DI Number

40026072011582

Quantity per Package

5

Contains DI Package

00026072011584

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case