Catalog Number

DYNJCTRST30ML

Brand Name

Medline Industries, Inc.

Version/Model Number

DYNJCTRST30ML

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K982123,K982123

Product Code

FPA

Product Code Name

Set, administration, intravascular

Public Device Record Key

d38c5d29-6fa2-44da-ae2f-720bcdd51cf2

Public Version Date

August 12, 2022

Public Version Number

1

DI Record Publish Date

August 04, 2022

Package DI Number

40889942856009

Quantity per Package

20

Contains DI Package

10889942856008

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE