Catalog Number

I68030

Brand Name

Centurion

Version/Model Number

I68030

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

GEN

Product Code Name

FORCEPS, GENERAL & PLASTIC SURGERY

Public Device Record Key

184501d3-e2b6-49eb-90a0-9dd544408e3d

Public Version Date

January 10, 2022

Public Version Number

1

DI Record Publish Date

January 01, 2022

Package DI Number

10653160228288

Quantity per Package

20

Contains DI Package

00653160228281

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE