Catalog Number

Durable Water Trap 22M

Brand Name

N/A

Version/Model Number

70106

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

-

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

BYH

Product Code Name

Drain, Tee (Water Trap)

Public Device Record Key

cf2436a2-075c-4fc9-a008-2a7a9b3f2835

Public Version Date

August 23, 2018

Public Version Number

3

DI Record Publish Date

October 15, 2015

Package DI Number

44710810084476

Quantity per Package

50

Contains DI Package

04710810084478

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton