Catalog Number

BIPMBLA

Brand Name

Dornier MedTech

Version/Model Number

Bipolar Medium Bladder Loop 24 Fr Electrode-Sterile, Single-Use. (6/box)

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KNF

Product Code Name

Coagulator-Cutter, Endoscopic, Unipolar (And Accessories)

Public Device Record Key

e1e21294-dad7-44ce-9c17-7ff96ce04b83

Public Version Date

June 29, 2020

Public Version Number

1

DI Record Publish Date

June 19, 2020

Package DI Number

00810116021758

Quantity per Package

6

Contains DI Package

00810116021680

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box