Catalog Number

V-2254

Brand Name

DEKNATEL

Version/Model Number

IPN026402

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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"

Yes

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

OVN

Product Code Name

Suture kit

Public Device Record Key

357c7c0a-1503-45b6-bac4-14c29bc8a13e

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 16, 2015

Package DI Number

24026704424959

Quantity per Package

12

Contains DI Package

04026704424955

Package Discontinue Date

March 09, 2018

Package Status

Not in Commercial Distribution

Package Type

Box