Catalog Number

0600-2160-000

Brand Name

Richard Wolf

Version/Model Number

0600-2160-000

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 10, 2020

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"

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

-

Product Code

HAO

Product Code Name

INSTRUMENT, SURGICAL, NON-POWERED

Public Device Record Key

60d34bab-d821-4edb-85e4-6804cc96c6af

Public Version Date

January 13, 2020

Public Version Number

2

DI Record Publish Date

January 29, 2019

Package DI Number

20817984011199

Quantity per Package

4

Contains DI Package

00817984011195

Package Discontinue Date

January 10, 2020

Package Status

Not in Commercial Distribution

Package Type

Case