Catalog Number

DYNDA2190

Brand Name

MEDLINE

Version/Model Number

DYNDA2190

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KDC

Product Code Name

INSTRUMENT, SURGICAL, DISPOSABLE

Public Device Record Key

2130b1c6-083f-4fa9-9366-80f3ff6158f8

Public Version Date

June 17, 2022

Public Version Number

2

DI Record Publish Date

October 11, 2021

Package DI Number

40889942805724

Quantity per Package

25

Contains DI Package

10889942805723

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE