Catalog Number

SN380

Brand Name

V. Mueller

Version/Model Number

SN380

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 15, 2021

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

-

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

GDO

Product Code Name

Applier, surgical, clip

Public Device Record Key

74eeede2-5648-4f1b-90d8-9f3009d623e9

Public Version Date

March 08, 2022

Public Version Number

3

DI Record Publish Date

February 08, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-