Catalog Number

TRAPJ 0810

Brand Name

TRAPSYSTEM SET

Version/Model Number

TRAPSYSTEM SET

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

K013692,K013692

Product Code

KNW

Product Code Name

Instrument, Biopsy

Public Device Record Key

7b5d6764-f53e-4736-9980-3a67cd31c1a9

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

September 26, 2016

Package DI Number

38033003347875

Quantity per Package

10

Contains DI Package

08033003347874

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-