Catalog Number

8-600

Brand Name

HU-FRIEDY

Version/Model Number

8-600

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

January 19, 2022

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

EFL

Product Code Name

FORCEPS, DRESSING, DENTAL

Public Device Record Key

64ce4ae1-ab1b-4135-867f-1023330de385

Public Version Date

January 20, 2022

Public Version Number

2

DI Record Publish Date

August 14, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-