Catalog Number

RH0871-1

Brand Name

V. Mueller

Version/Model Number

RH0871-1

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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"

-

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

EMF

Product Code Name

KNIFE, SURGICAL

Public Device Record Key

bcfa6a17-da24-4606-8801-cd84e695a01c

Public Version Date

January 22, 2021

Public Version Number

3

DI Record Publish Date

September 10, 2018

Package DI Number

70885403128983

Quantity per Package

6

Contains DI Package

10885403128981

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Pack