Catalog Number

-

Brand Name

FibriJet

Version/Model Number

SA-3670

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

-

Product Code

KYZ

Product Code Name

Syringe, Irrigating (Non Dental)

Public Device Record Key

3ea161c4-864d-42e8-b695-a58a98c06ab3

Public Version Date

September 13, 2022

Public Version Number

2

DI Record Publish Date

June 07, 2022

Package DI Number

10815634021676

Quantity per Package

10

Contains DI Package

00815634021679

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Pack