Catalog Number

MNS13850

Brand Name

Centurion Medical Products Corp

Version/Model Number

MNS13850

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

MDM

Product Code Name

INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Public Device Record Key

7487335d-9137-4645-bcc2-8aff8fb398cc

Public Version Date

July 25, 2022

Public Version Number

1

DI Record Publish Date

July 17, 2022

Package DI Number

40653160993330

Quantity per Package

20

Contains DI Package

10653160993339

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE