Catalog Number

GGS5660F

Brand Name

Glide & Guide Turn Sheet Select

Version/Model Number

GGS5660F

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FMR

Product Code Name

Device, Transfer, Patient, Manual

Public Device Record Key

e5d0a901-94a3-4eec-a1d1-04bba9a6d41b

Public Version Date

September 09, 2020

Public Version Number

2

DI Record Publish Date

February 27, 2019

Package DI Number

00810006680812

Quantity per Package

5

Contains DI Package

00810006680423

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE