PENTAX ENDO SMARTCAP - Pentax Endo Smartcap - MEDIVATORS INC.

Duns Number:068199363

Device Description: Pentax Endo Smartcap

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More Product Details

Catalog Number

-

Brand Name

PENTAX ENDO SMARTCAP

Version/Model Number

100150CO2P

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 03, 2022

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

FAJ

Product Code Name

Cystoscope And Accessories, Flexible/Rigid

Device Record Status

Public Device Record Key

8d8d0343-7ed7-4b26-99ba-f7da46d49ed9

Public Version Date

June 10, 2022

Public Version Number

6

DI Record Publish Date

October 10, 2018

Additional Identifiers

Package DI Number

20677964060339

Quantity per Package

50

Contains DI Package

00677964060335

Package Discontinue Date

May 03, 2022

Package Status

Not in Commercial Distribution

Package Type

Case

"MEDIVATORS INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 2999
2 A medical device with a moderate to high risk that requires special controls. 362