Catalog Number

URHT19

Brand Name

Biotronix Healthcare

Version/Model Number

URHT19

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

KYZ

Product Code Name

Syringe, Irrigating (Non Dental)

Public Device Record Key

f1dff05e-6800-4ba0-a534-326f100ad480

Public Version Date

December 24, 2019

Public Version Number

2

DI Record Publish Date

October 04, 2019

Package DI Number

10850005165047

Quantity per Package

20

Contains DI Package

00850005165040

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-