Catalog Number

M.27.03.E200

Brand Name

StecoGuide

Version/Model Number

M.27.03.E200

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NDP

Product Code Name

Accessories, Implant, Dental, Endosseous

Public Device Record Key

366457a1-50ed-4268-be4b-5849947efd69

Public Version Date

August 09, 2019

Public Version Number

4

DI Record Publish Date

May 03, 2018

Package DI Number

M2703E2002

Quantity per Package

1

Contains DI Package

ESTOM2703E2000

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

foil pouch