Catalog Number

506410P22G

Brand Name

RAIN Sheath Transradial

Version/Model Number

506410P22G

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"

-

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

f20fdda6-d2ec-413e-8239-ad972d07f939

Public Version Date

August 12, 2022

Public Version Number

4

DI Record Publish Date

December 17, 2020

Package DI Number

20705032082263

Quantity per Package

5

Contains DI Package

10705032082266

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX