Catalog Number

321BCA

Brand Name

MiniMedicut™

Version/Model Number

321BCA

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LRW

Product Code Name

Scissors, General, Surgical

Public Device Record Key

7297557f-a6ba-4a2c-9311-d46ac72a6512

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 28, 2016

Package DI Number

00634782584511

Quantity per Package

16

Contains DI Package

00634782884512

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Case