Catalog Number

-

Brand Name

N/A

Version/Model Number

MFR 49 TIP II 1 ea

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

202d7eb7-f5dd-48ca-89af-3850d2b2b3ff

Public Version Date

July 26, 2021

Public Version Number

4

DI Record Publish Date

September 09, 2016

Package DI Number

8809447651040

Quantity per Package

1

Contains DI Package

08809447651033

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box