Catalog Number

-

Brand Name

WOLF Devortex Reload Pack, 8F

Version/Model Number

FD0427-14

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

QEW

Product Code Name

Peripheral Mechanical Thrombectomy With Aspiration

Public Device Record Key

f2c8acb9-85c7-4e01-be5c-d37a2512c11d

Public Version Date

October 24, 2022

Public Version Number

2

DI Record Publish Date

October 12, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-