Catalog Number

G60235260

Brand Name

Mermaid Medical® Guidewire

Version/Model Number

G60235260

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

K053251,K053251

Product Code

DQX

Product Code Name

Wire, Guide, Catheter

Public Device Record Key

aab2ed3f-49a0-4645-b605-4dc360c7a13f

Public Version Date

December 22, 2021

Public Version Number

5

DI Record Publish Date

September 23, 2016

Package DI Number

20850758007080

Quantity per Package

10

Contains DI Package

00850758007086

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box