Catalog Number

-

Brand Name

UNIVERSAL PLUS

Version/Model Number

UP18250-00

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

K092338,K092338

Product Code

KNW

Product Code Name

Instrument, Biopsy

Public Device Record Key

12477014-fef3-4801-9be3-804ea742aaf8

Public Version Date

July 06, 2018

Public Version Number

2

DI Record Publish Date

April 10, 2018

Package DI Number

18056515880308

Quantity per Package

10

Contains DI Package

08056515880301

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-