Catalog Number

-

Brand Name

Cramer Tape Remover

Version/Model Number

201033

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

KOX

Product Code Name

Solvent, Adhesive Tape

Public Device Record Key

09ab5552-049d-4d6d-80d8-523909fa1aae

Public Version Date

March 11, 2019

Public Version Number

2

DI Record Publish Date

October 01, 2018

Package DI Number

10311960439098

Quantity per Package

12

Contains DI Package

00311960439091

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Carton