Catalog Number

ICM-000-0418

Brand Name

Speculum Tubing

Version/Model Number

2195

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"

Yes

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

GEX

Product Code Name

Powered Laser Surgical Instrument

Public Device Record Key

44d6779e-23e1-42ac-8346-885bdc3d8163

Public Version Date

April 08, 2019

Public Version Number

5

DI Record Publish Date

September 24, 2016

Package DI Number

00817688021421

Quantity per Package

25

Contains DI Package

00817688021414

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-