Catalog Number

-

Brand Name

Single Use Biopsy Forceps

Version/Model Number

MD-A-BF2423

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

FCL

Product Code Name

Forceps, Biopsy, Non-Electric

Public Device Record Key

2965c0d9-2f78-4984-8489-0be58dbf727f

Public Version Date

July 18, 2022

Public Version Number

3

DI Record Publish Date

December 03, 2018

Package DI Number

26970401813517

Quantity per Package

10

Contains DI Package

16970401813503

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case