Catalog Number

-

Brand Name

Anästhesie Set ID Coax Watertrap 210

Version/Model Number

MP03388

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

BTC

Product Code Name

Bag, Reservoir

Public Device Record Key

3844b4cc-1459-441e-88ba-95725a4c7529

Public Version Date

October 24, 2022

Public Version Number

3

DI Record Publish Date

November 19, 2018

Package DI Number

04048675552635

Quantity per Package

10

Contains DI Package

04048675552628

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-