Catalog Number

-

Brand Name

Single Use Cannula V

Version/Model Number

PR-V223Q

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

K950729,K950729

Product Code

ODD

Product Code Name

Endoscopic retrograde cholangiopancreatography (ERCP) cannula

Public Device Record Key

658c0789-2414-4c2d-89a0-9532c96ae9a6

Public Version Date

November 19, 2020

Public Version Number

4

DI Record Publish Date

September 21, 2016

Package DI Number

14953170183697

Quantity per Package

1

Contains DI Package

04953170183690

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-