Ureteral Access Sheath with 2, 3 Fr working channels dilator, 10 Fr x 35cm - Promepla

Duns Number:401020409

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More Product Details

Catalog Number

ROUS1035ST

Brand Name

Ureteral Access Sheath with 2, 3 Fr working channels dilator, 10 Fr x 35cm

Version/Model Number

09-0015

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

-

Product Code Details

Product Code

KNY

Product Code Name

Accessories, Catheter, G-U

Device Record Status

Public Device Record Key

a014e8dc-39d0-4300-9771-3052580bf655

Public Version Date

December 09, 2019

Public Version Number

5

DI Record Publish Date

November 09, 2017

Additional Identifiers

Package DI Number

03700512986195

Quantity per Package

5

Contains DI Package

03700512976196

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"PROMEPLA" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 64
2 A medical device with a moderate to high risk that requires special controls. 152