Catalog Number

-

Brand Name

Tech-Medical Services

Version/Model Number

TM102

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

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

NKC

Product Code Name

Tubing/Tubing With Filter, Insufflation, Laparoscopic

Public Device Record Key

d04cd0ad-6fa2-4e7c-a9cd-fc0dac2ba180

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

May 03, 2021

Package DI Number

10851695005064

Quantity per Package

10

Contains DI Package

00851695005067

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box