Catalog Number

1023S-50

Brand Name

MORRISON MEDICAL

Version/Model Number

1023S-50

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NOD

Product Code Name

Board, Arm (With Cover), Non-Sterile

Public Device Record Key

69529c8d-be1b-47b3-b72c-25bbfc4eace8

Public Version Date

November 15, 2019

Public Version Number

2

DI Record Publish Date

November 06, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-