Catalog Number

-

Brand Name

Blom

Version/Model Number

313-50-060

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,K062104

Product Code

BTO

Product Code Name

Tube, Tracheostomy (W/Wo Connector)

Public Device Record Key

4ad42a3c-405e-4718-b029-b3d8e2b72914

Public Version Date

June 05, 2020

Public Version Number

4

DI Record Publish Date

November 06, 2015

Package DI Number

20841470100616

Quantity per Package

100

Contains DI Package

10841470100619

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-