Catalog Number

J1310

Brand Name

BMN J TYPE

Version/Model Number

BMN J TYPE

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

K013070,K013070

Product Code

KNW

Product Code Name

Instrument, Biopsy

Public Device Record Key

eadab8ac-bb4d-4d1f-b4ef-874a1649e310

Public Version Date

December 26, 2019

Public Version Number

1

DI Record Publish Date

December 18, 2019

Package DI Number

38033003344614

Quantity per Package

10

Contains DI Package

08033003344613

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-