Catalog Number

04-4105

Brand Name

EndoSheath Technology

Version/Model Number

BF-0

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

K091768,K091768

Product Code

EOQ

Product Code Name

Bronchoscope (Flexible Or Rigid)

Public Device Record Key

f14fb338-01c8-4846-8543-b6fd65c5ecaf

Public Version Date

November 10, 2021

Public Version Number

6

DI Record Publish Date

September 23, 2016

Package DI Number

20874485001562

Quantity per Package

10

Contains DI Package

00874485003050

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-