Catalog Number

-

Brand Name

INSTRUSAFE

Version/Model Number

OM-1000-MU

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"

Yes

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K051157,K133015,K140289,K141513,K142630,K142768,K150540,K151166,K051157,K133015,K140289,K141513,K142630,K142768,K150540,K151166

Product Code

KCT

Product Code Name

Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Public Device Record Key

54e4146b-cd76-43eb-80a7-f134e2ea13aa

Public Version Date

September 16, 2022

Public Version Number

6

DI Record Publish Date

July 08, 2020

Package DI Number

10385640053447

Quantity per Package

25

Contains DI Package

00385640053440

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box