Catalog Number

-

Brand Name

Replacement attachments for Durette® III (set of 8)

Version/Model Number

21-440

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

Yes

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

-

FDA Premarket Submission

-

Product Code

IWS

Product Code Name

Shield, Eye, Radiological

Public Device Record Key

c352b701-6e95-40c4-af78-e01335840205

Public Version Date

November 19, 2019

Public Version Number

1

DI Record Publish Date

November 11, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-