Catalog Number

8208CS

Brand Name

POSEY

Version/Model Number

8208CS

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KMI

Product Code Name

Monitor, Bed Patient

Public Device Record Key

e4ed5b43-3164-45a4-9e92-77a7b6685f92

Public Version Date

October 12, 2022

Public Version Number

1

DI Record Publish Date

October 04, 2022

Package DI Number

20190676004526

Quantity per Package

20

Contains DI Package

10190676004529

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case