Catalog Number

BM 2010

Brand Name

BIOMOL

Version/Model Number

BIOMOL

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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"

Yes

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

K002947,K002947,K002947

Product Code

FCG

Product Code Name

Biopsy Needle

Public Device Record Key

20695f67-ed28-45f8-9433-28b9c208f1a3

Public Version Date

October 14, 2021

Public Version Number

5

DI Record Publish Date

September 26, 2016

Package DI Number

28033003340701

Quantity per Package

5

Contains DI Package

08033003340707

Package Discontinue Date

March 15, 2019

Package Status

Not in Commercial Distribution

Package Type

-