Catalog Number

DMR190704

Brand Name

2F AND 3F VASCU-SHEATH TEARAWAY INTRODUCER2F AND 3F VASCU-SHEATH TEARAWAY INTROD

Version/Model Number

DMR190704

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

DYB

Product Code Name

INTRODUCER, CATHETER

Public Device Record Key

e186351d-6bc7-4441-89a0-5aeaed879a29

Public Version Date

June 14, 2019

Public Version Number

1

DI Record Publish Date

June 06, 2019

Package DI Number

50884908143749

Quantity per Package

4

Contains DI Package

30884908143745

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box