Catalog Number

-

Brand Name

Reicodent

Version/Model Number

02-1086-11 C

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

-

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

HXK

Product Code Name

Holder, Needle; Orthopedic

Public Device Record Key

e5b73837-6a4e-47f5-a276-b5dc0f4d7c0f

Public Version Date

January 08, 2021

Public Version Number

2

DI Record Publish Date

December 29, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-