Catalog Number

11

Brand Name

MANI Sutures Silk

Version/Model Number

11

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

GAP

Product Code Name

Suture, Nonabsorbable, Silk

Public Device Record Key

cfa7a92b-9485-4332-8dd0-135a30f31357

Public Version Date

October 18, 2021

Public Version Number

8

DI Record Publish Date

March 25, 2016

Package DI Number

14546951500020

Quantity per Package

12

Contains DI Package

04546951500023

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-