Porges Coloplast - FOLYSIL® Foley catheter for neobladder silicone - Coloplast A/S

Duns Number:305524696

Device Description: FOLYSIL® Foley catheter for neobladder silicone CH FR 20

Want to know more about this Product? Request more information now!


More Product Details

Catalog Number

AA6820

Brand Name

Porges Coloplast

Version/Model Number

AA6820

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

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"

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

K013174,K013174

Product Code Details

Product Code

EZL

Product Code Name

CATHETER, RETENTION TYPE, BALLOON

Device Record Status

Public Device Record Key

7d0e8b7b-7dbe-486d-98c2-8f53428e38ad

Public Version Date

December 04, 2020

Public Version Number

9

DI Record Publish Date

September 22, 2016

Additional Identifiers

Package DI Number

03600040131657

Quantity per Package

5

Contains DI Package

03600040131640

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Retail box

"COLOPLAST A/S" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 46
2 A medical device with a moderate to high risk that requires special controls. 899
3 A medical device with high risk that requires premarket approval 72
U Unclassified 7