DeRoyal - 3 PORT MANIFOLD RA RH ON W/ 20 in EXTENSION TBG - DEROYAL INDUSTRIES, INC.

Duns Number:096372255

Device Description: 3 PORT MANIFOLD RA RH ON W/ 20 in EXTENSION TBG

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More Product Details

Catalog Number

35-401069

Brand Name

DeRoyal

Version/Model Number

35-401069

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

DXT

Product Code Name

Injector and syringe, angiographic

Device Record Status

Public Device Record Key

bd3fb88f-7961-4736-a8f0-c4b7589713c0

Public Version Date

August 31, 2021

Public Version Number

1

DI Record Publish Date

August 23, 2021

Additional Identifiers

Package DI Number

50749756927609

Quantity per Package

20

Contains DI Package

00749756927604

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case

"DEROYAL INDUSTRIES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 7041
2 A medical device with a moderate to high risk that requires special controls. 4913
U Unclassified 3