5530 3L SYRINGE - iCardiac 3L SYRINGE 5530 - HANS RUDOLPH, INC.

Duns Number:007131725

Device Description: iCardiac 3L SYRINGE 5530

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More Product Details

Catalog Number

113863

Brand Name

5530 3L SYRINGE

Version/Model Number

5530

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"

-

For Single-Use

-

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

BXW

Product Code Name

Calibrator, Volume, Gas

Device Record Status

Public Device Record Key

d797806b-64e3-48f9-a6df-1695eeec5cf4

Public Version Date

December 06, 2018

Public Version Number

1

DI Record Publish Date

November 05, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"HANS RUDOLPH, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 922
2 A medical device with a moderate to high risk that requires special controls. 407