Catalog Number

D1005

Brand Name

Tego™

Version/Model Number

D1005

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K053106,K053106

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

ea1dee6b-2a09-40de-b0d4-bcd9ed2a2568

Public Version Date

July 27, 2021

Public Version Number

1

DI Record Publish Date

July 19, 2021

Package DI Number

10840619069213

Quantity per Package

100

Contains DI Package

00840619069216

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS