Catalog Number

-

Brand Name

Blom

Version/Model Number

313-10-080

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K062104,K062104

Product Code

BTO

Product Code Name

Tube, Tracheostomy (W/Wo Connector)

Public Device Record Key

e11cb9cd-def6-4e81-ae7d-b773a378d443

Public Version Date

June 05, 2020

Public Version Number

4

DI Record Publish Date

November 13, 2015

Package DI Number

10841470103191

Quantity per Package

10

Contains DI Package

00841470103194

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-